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CTRI Number  CTRI/2020/09/027854 [Registered on: 17/09/2020] Trial Registered Prospectively
Last Modified On: 04/11/2020
Post Graduate Thesis  No 
Type of Trial  Interventional 
Type of Study   Surgical/Anesthesia
Dentistry 
Study Design  Randomized, Parallel Group Trial 
Public Title of Study   To check efficacy of nerve block technique for pain relief in management of oral infection and jaw fracture 
Scientific Title of Study   EFFICACY OF SUPERFICIAL CERVICAL PLEXUS NERVE BLOCK IN MANAGEMENT OF MANDIBULAR FRACTURES AND PERIMANDIBULAR SPACE INFECTION- A RANDOMIZED CLINICAL TRIAL. 
Trial Acronym   
Secondary IDs if Any  
Secondary ID  Identifier 
NIL  NIL 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Prajwalit Prakash Kende 
Designation  Professor and HOD 
Affiliation  Government dental college and hospital Mumbai 
Address  Room No 126, Department of Oral and Maxillofacial Surgery, 1st floor, Government Dental College and Hospital, Near CST, PD Mello road Mumbai-400001

Mumbai
MAHARASHTRA
400001
India 
Phone  09324715824  
Fax    
Email  prajwalitkende1979@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  Dr Prajwalit Kende 
Designation  Professor and head 
Affiliation  Government dental college and hospital Mumbai 
Address  Department of oral and maxillofacial surgery Government dental college and hospital Saint George hospital campus P D Mellow road Fort Mumbai

Mumbai
MAHARASHTRA
400001
India 
Phone  09324715824  
Fax    
Email  prajwalitkende1979@gmail.com  
 
Details of Contact Person
Public Query
 
Name  Maroti Baburao Wadewale 
Designation  Postgraduate student 
Affiliation  Government dental college and hospital Mumbai 
Address  room No 126, Department of Oral and Maxillofacial Surgery, Government Dental College and Hospital, St George hospital campus, PDS Mello road, near cst, Fort Mumbai-400001

Mumbai
MAHARASHTRA
400001
India 
Phone  08483851334  
Fax    
Email  dr.marotiwadewale59@gmail.com  
 
Source of Monetary or Material Support  
Department of Oral and Maxillofacial Surgery Government Dental College and Hospital Mumbai 
 
Primary Sponsor  
Name  Government dental college and hospital Mumbai 
Address  Government dental college and hospital, Saint George hospital campus P D Mellow road Near CST Fort Mumbai 400001 
Type of Sponsor  Other [Government dental college] 
 
Details of Secondary Sponsor  
Name  Address 
NIL  NIL 
 
Countries of Recruitment     India  
Sites of Study  
No of Sites = 1  
Name of Principal Investigator  Name of Site  Site Address  Phone/Fax/Email 
Maroti Wadewale  Government dental college and hospital Mumbai  Government dental college and hospital Saint George hospital campus P D Mellow road Near CST Fort Mumbai
Mumbai
MAHARASHTRA 
8483851334

dr.marotiwadewale59@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
institutional Ethics committee  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition: S026||Fracture of mandible, (2) ICD-10 Condition: A418||Other specified sepsis,  
 
Intervention / Comparator Agent  
Type  Name  Details 
Comparator Agent  2% Lignocaine with adrenaline (1:80000)  Infilteration will be given 
Intervention  2% Lignocaine with adrenaline (1:80000)  with the use of local anaesthetic agent superficial cervical plexus nerve block will be given 
 
Inclusion Criteria  
Age From  18.00 Year(s)
Age To  60.00 Year(s)
Gender  Both 
Details  1. Patients are willing to participate in the study.
2. Patients with mandibular fractures and/or with perimandibular space infection.
3. Patients are willing for surgery under local anesthesia.
4. American Society of Anaesthesiology I or II patients. 
 
ExclusionCriteria 
Details  1. A patient with any other associated Cranio-maxillary fractures except mandibular fractures.
2. Patients with facial space infection other than perimandibular space infection.
3. Patients with condylar fractures.
4. Patients having a history of any systemic diseases.
5. Pregnant and lactating patient.
6. Patients who do not want the procedure to be done under regional anesthesia, and patients with a
history of allergy to the local anesthetic.
7. Patients who are unable to follow study protocol. 
 
Method of Generating Random Sequence   Computer generated randomization 
Method of Concealment   An Open list of random numbers 
Blinding/Masking   Not Applicable 
Primary Outcome  
Outcome  TimePoints 
1) Assessing Pain after superficial cervical plexus nerve block or infiltration immediately,
intraoperative and immediate postoperatively will be assessed on VAS scale.
2) Time of onset of anesthesia.
3) Duration of anesthesia.
4) Time interval until first analgesic request.
5) Intraoperative analgesic/anaesthetic requirements.
6) Pulse and blood pressure preoperatively and intraoperative at 10 minutes and 30
minutes of interval. 
1) immediately, intraoperative and immediate postoperatively.
2) Immediately
3) Immediately
4) Time interval until first analgesic request.
5) Intraoperative analgesic/anaesthetic requirements.
6) preoperatively and intraoperative at 10 minutes and 30 minutes of interval. 
 
Secondary Outcome  
Outcome  TimePoints 
Any other complications.  IMMEDIATE AND POSTEOPERATIVELY TILL 1 WEEK 
 
Target Sample Size   Total Sample Size="24"
Sample Size from India="24" 
Final Enrollment numbers achieved (Total)= "24"
Final Enrollment numbers achieved (India)="24" 
Phase of Trial   Phase 4 
Date of First Enrollment (India)   21/09/2020 
Date of Study Completion (India) 30/10/2020 
Date of First Enrollment (Global)  Date Missing 
Date of Study Completion (Global) 30/10/2020 
Estimated Duration of Trial   Years="0"
Months="5"
Days="5" 
Recruitment Status of Trial (Global)
Modification(s)  
Not Applicable 
Recruitment Status of Trial (India)  Completed 
Publication Details   5. Moshe Shteif et al. The Use of the Superficial Cervical Plexus Block in the Drainage of Submandibular and Submental Abscesses—An Alternative for General Anesthesia. J Oral Maxillofac Surg 66:2642-2645, 2008 9. Kamal Kanthan R. The use of superficial cervical plexus block in oral and maxillofacial surgical practice as an alternative to general anesthesia in selective cases. Annals of Maxillofacial Surgery | January - June 2016 | Vol-6 Issue 1 
Individual Participant Data (IPD) Sharing Statement

Will individual participant data (IPD) be shared publicly (including data dictionaries)?  

Response - NO
Brief Summary
Modification(s)  

INTRODUCTION-

Pain is conducted in the nervous system originated with the specific theory of Johannes P. Müller, described in 1826. This was followed by the alternate intensity theory of Erb in 1874 (Dallenbach, 1939), an idea that later culminated in the gate theory of pain by Melzack and Wall in 1965. Anesthesia is the partial or complete loss of sensation, with or without loss of consciousness. Regional anesthesia is a type of pain management for surgery that numbs a large part of the body1. Regional anesthesia is very safe and doesn’t involve the potential complications and side effects that can happen with sedation and general anesthesia1.

Trauma is one of the leading causes of death amongst the population under the age of 40 years2. The main causes of maxillofacial fractures worldwide are traffic accidents, assaults, falls, and sport-related injuries2. The mandible is the second most common facial fracture3. Odontogenic infection is the most prevalent disease worldwide and is the principal reason for seeking dental care. The commonest odontogenic infections are periapical abscess, pericoronitis, and periodontal abscess. Spreading odontogenic infections are the most common type of serious oro-facial infections encountered by oral and maxillofacial surgeons. Infection from the original focus can spread along with the tissue spaces and lead to facial cellulitis involving deeper fascial spaces4. Submandibular space was the most common primary space involved (46.45%) followed by buccal space (30.32%) 4. Mandibular fractures and facial space infections can be treated under general anesthesia, sedation, local anesthesia, sedation, and local anesthesia.

General anesthesia has its downsides high economic cost, a number of highly trained personnel required, morbidity and mortality, and high-cost equipment5. On the other hand, regional anesthesia has a number of advantages: Stress-free anesthesia, Lower rates of postoperative pulmonary embolism and thrombosis, Easy to perform techniques, and Lower morbidity rates. The regional anesthesia of the superficial cervical plexus (SCP) is commonly and frequently used in a variety of disciplines like carotid endarterectomy, thyroid surgeries, vocal cord surgeries etc6-8. Many techniques can be employed to achieve anesthesia of the dentition and surrounding hard and soft tissues of the maxilla and mandible. The superficial cervical plexus block (SCPB) is simple and easy to perform, but unfortunately, it is often overlooked as an option to general anesthesia11. Its application in oral and maxillofacial surgical (OMFS) has been in surgical drainage of an abscess in the perimandibular region, excisions of superficial lesions, skin suturing in the corresponding dermatome, and in management of mandibular fractures5, 9-10

We will be conducting a prospective, cohort Randomised Controlled Trials (RCT) to evaluate the EFFICACY OF SUPERFICIAL CERVICAL PLEXUS NERVE BLOCK IN MANAGEMENT OF MANDIBULAR FRACTURES AND PERIMANDIBULAR SPACE INFECTION.

 

SIGNIFICANCE OF THE STUDY

      I.         Superficial cervical plexus nerve block delivers analgesia which decreases the time of surgery.

     II.         Risks and complications of general anesthesia (GA) is avoided.

   III.         Pain management during the treatment of mandibular fractures and perimandibular space infection will be more precise.

 

REVIEW OF LITERATURE

1.     Michael F. Mulroy MDChristopher M. Bernards MDSusan B. McDonald MD,Francis V. Salinas.-A Practical Approach to Regional Anesthesia Fourth Edition1.

2.     Moshe Shteif et al. The Use of the Superficial Cervical Plexus Block in the Drainage of Submandibular and Submental Abscesses—An Alternative for General Anesthesia. J Oral Maxillofac Surg 66:2642-2645, 2008

3.     Roger D (1995) Superficial and deep cervical plexus block: technical considerations. J Am Assoc Nurse Anesth 63(3):235–24311.

4.     Tajamul Ahmad Hakim et al. The Safety and Effectiveness of Superficial Cervical Plexus Block in Oral and Maxillofacial Surgery as an Alternative to General Anesthesia in Selective Cases: A Clinical Study. J. Maxillofac. Oral Surg. DOI 10.1007/s12663-017-1029-410.

5.     Kamal Kanthan R. The use of superficial cervical plexus block in oral and maxillofacial surgical practice as an alternative to general anesthesia in selective cases. Annals of Maxillofacial Surgery | January - June 2016 | Vol-6 Issue 19.


AIM-

To evaluate the efficacy of superficial cervical plexus nerve block in the management of mandibular fractures and perimandibular space infection.

 

OBJECTIVES-

1.     To study pain immediately after block, intraoperative, and immediately postoperatively on the VAS scale.

2.     To evaluate the time of onset anesthesia.

3.     Check the duration of anesthesia.

4.     To evaluate the time interval until the first analgesic request.

5.     To evaluate Intraoperative analgesic/anesthetic requirements.

6.     To evaluate changes in the pulse and blood pressure preoperatively and intraoperative at two intervals after 15 minutes and after 30 minutes of giving block/infiltration.

7.     To check the complications of SCNB and infiltrations.

 

TYPE OF STUDY- a Prospective, Randomised Clinical Trial (RCT)

MATERIAL & METHODOLOGY-

STUDY DESIGN-

Ø  This prospective, cohort, Randomised Clinical Trial (RCT)-Double blind study will be conducting the Department of Oral & Maxillofacial Surgery, Government Dental College & Hospital, Mumbai from July 2019.

Ø  The study population will be selected by randomization from the outpatient department (OPD) of Dept. Oral and Maxillofacial Surgery, Govt. Dental College and Hospital, Mumbai which will be divided into two arms (control arm (CA) & experimental arm (EA). Minimum 12 patients in each group will be included, as per the sample size formulae used as follows: (statistician sample certificate is attached)

                        n   =            2 (Zα+ Zβ)2  [s]2

                                                     d2

 

where Zα is the z variate of alpha error i.e. a constant with value 1.96, Zβ  is the z variate of beta error i.e. a constant with value 0.84

(Reference: Allen JC. Sample Size Calculation for Two Independent Groups: A Useful Rule of Thumb. Proceedings of Singapore Healthcare 2011:20(2); 138-40) 

Approximate estimates: 

  1. 80% power 
  2. Type I error to be 5%
  3. Type II error to be 20%
  4. The true difference of at least 2.1 units between the groups 
  5. The pooled standard deviation of 1.8

Substituting the values,

                       n   =                        2 (2.8)2  [1.8]2

                                                             (2.1)2

 

                                              n = 11.52

Approximately 12 subjects per group need to be taken in the present study. 

 

NOTE: Sample Size estimates indicate the minimum no of subjects/samples to be recruited in the study, however they do not guarantee whether statistical significance may be achieved or not as it depends on various other factors also.

For follow-up studies, to avoid loss by loss to follow up / attrition, kindly consider recruiting 5-25% more subjects so that even after attrition, we would be able to achieve the required minimum sample size.

PROCEDURE DETAILS

A)    Control Arm (CA):

                                Under all aseptic precautions and standard aseptic protocol Patients in the control arm will be treated under indicated nerve block and infiltration externally in the skin. After the management of mandibular fracture and/or perimandibular space infection Postoperative medications will be prescribed and written instructions will be given to the patient.

 

B)    Experimental Arm (EA):

Under all aseptic precautions and standard aseptic protocol Patients in the experimental arm will be treated under indicated nerve block and superficial cervical plexus nerve block (SCNB). 

PATIENT POSITIONING

The patient is placed in a supine position, with his head turned to the side contrary to the one to be blocked. After skin cleansing with an antiseptic solution, a skin wheel is raised at the site of the needle insertion using a 25-gauge needle. Next, using a “fan” technique with superior-inferior needle redirections, the local anesthetic is injected alongside the posterior border of the sternocleidomastoid muscle, 2 to 3 cm below and above the needle insertion site. This injection technique should be adequate to achieve blockade of all 4 major branches of the SCP. After the management of mandibular fracture and/or perimandibular space infection Postoperative medications will be prescribed and written instructions will be given to the patient.

DATA ANALYSIS

·      Data collected will be compiled on to an MS Office excel worksheet and will be subjected to statistical analysis using an appropriate package like SPSS software.

·      Normality of data will be checked using the Shapiro – Wilk test or Kolmogorov-Smirnov test. Depending on the normality of data, statistical tests will be determined. 

·      For a numerical continuous data following a normal distribution, intergroup comparison (2 groups) will be done using an appropriate test, else a non-parametric substitute like appropriate test will be used. 

·      Association of variables (2 categorical) will be done using a suitable test.

·      Intragroup comparisons for a numerical continuous data following a normal distribution will be done by applying appropriate test (for observations), else a non-parametric substitute like Wilcoxon signed-rank test (for 2 observations) or Friedman’s test for >2 observations will be used. 

·      Keeping alpha error at 5% and Beta error at 20%, power at 80%, p<0.05 will be considered statistically significant. 


FINDINGS OF TRIAL-

masterchart of variabless measured


Sr. No.Randomization No.GroupAge/SexDiagnosisAetiologyTime of onset (sec)PainDurationintraop analgesicFirst analgesicPulseBP(systolic/diastolic)
 ImmediateIntraoppost op PREOPINTRAOPINTRAOP 2PREOPINTRAOPINTRAOP 2
11control22/MLeft Angle fractureRTA1235745yes197784104116/86120/88128/84
28control21Mleft Submandibular space infe tionOdontogenic infection1424830yes3827496124/84144/102140/94
315control30/Mright parasymphysis fractureFall5141038yes57479103130/86164/96170/90
421control35/Fludwigs anginaOdontogenic infection3251041yes6.5869194128/78136/86140/84
519control32/Fleft parasymphysis fractureRTA1045725yes86880101100/82110/86120/90
66Experimental19/Mrt parasymphysis fractureAsualt15634636yes208893100138/76142/80160/80
77Experimental20/Mleft angle left parasymphysis fractureRTA7623452no10768093122/72124/76132/80
82control22/Mright submandibular submental space infectionOdontogenic infection1423548no5688386110/74110/76120/84
911Experimental27/Fleft body fractureRTA9034454yes23547881132/76136/82142/96
1018Experimental36/Mright Angle fractureRTA12414548yes19667487136/78140/82164/90
1123Experimental44/Mright submandibular submental space infectionOdontogenic infection11025557no227479101118/82114/74136/88
1210Experimental39/Mright parasymphysis fractureRTA11223646no17849094120/80102/76124/86
135control52/Mludwigs anginaOdontogenic infection714436yes8798599124/84110/80126/102
1414control34/Mright body right parasymphysis fractureFall833748no1290102109132/82102/74140/80
154control29/Mright submandibular submental space infectionOdontogenic infection825642yes874110121126/88120/76126/80
1620Experimental34/FLeft Angle fractureRTA13413468no14727983134/80130/64136//92
1712Experimental39/FLeft Angle fractureRTA21314557no178084101124/76112/68120/90
1824Experimental21/Msubmental space infetionOdontogenic infection19413644no35647081120/80116/78152/84
1913control39/Fleft parasymphysis fractureRTA1528820yes7749097122/74130/78134/82
2017Experimental36/Mright  body fractureRTA19613649no18708487130/80130/74144/88
2122control39/FLeft Angle fractureRTA624733yes47480103124/80126/84124/90
223control41/Mright parasymphysis fractureRTA1312920yes1727684120/80120/80164/98
2316Experimental32/Mleft parasymphysis fractureRTA13423647no1848091126/74120/64130/70
249Experimental19/Mrifght submandibular + sublingual space infectionOdontogenic infection31223551yes148084114126/84120/82144/86

                  


 
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