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CTRI Number  CTRI/2023/07/055549 [Registered on: 24/07/2023] Trial Registered Prospectively
Last Modified On: 17/05/2025
Post Graduate Thesis  Yes 
Type of Trial  Interventional 
Type of Study   Drug 
Study Design  Randomized, Parallel Group, Active Controlled Trial 
Public Title of Study   Comparison between an injection treatment of botulinum toxin A and an oral tablet glycopyrrolate in patients of cerebral dysfunction with complaints ofexcessive salivation 
Scientific Title of Study   A comparative study on efficacy between ultrasound-guided botulinum toxin type a injection to salivary glands and oral glycopyrrolate therapy for management of sialorrhea in cerebral palsy 
Trial Acronym  Nil 
Secondary IDs if Any  
Secondary ID  Identifier 
NIL  NIL 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Indrajit De 
Designation  Post Graduate Traniee 
Affiliation  Institute of Postgraduate Medical Education and Research 
Address  Department of Physical Medicine and Rehabilitation Institute of Postgraduate Medical Education and Research 244 AJC Bose Road, Kolkata- 700020

Kolkata
WEST BENGAL
700020
India 
Phone  8145549644  
Fax    
Email  indrajitde.id@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  Firdaus Kamal 
Designation  Professor 
Affiliation  Institute of Postgraduate Medical Education and Research 
Address  Department of Physical Medicine and Rehabilitation Institute of Postgraduate Medical Education and Research 244 AJC Bose Road, Kolkata

Kolkata
WEST BENGAL
700020
India 
Phone  9830219554  
Fax    
Email  kamal.firdaus.kamal@gmail.com  
 
Details of Contact Person
Public Query
 
Name  Firdaus Kamal 
Designation  Professor 
Affiliation  Institute of Postgraduate Medical Education and Research 
Address  Department of Physical Medicine and Rehabilitation Institute of Postgraduate Medical Education and Research 244 AJC Bose Road, Kolkata


WEST BENGAL
700020
India 
Phone  9830219554  
Fax    
Email  kamal.firdaus.kamal@gmail.com  
 
Source of Monetary or Material Support  
Institute of Postgraduate Medical Education and Research 
 
Primary Sponsor  
Name  Institute of Postgraduate Medical Education and Research 
Address  Institute of Post Graduate Medical Education and Research 244 AJC Bose Road, Kolkata-700020 
Type of Sponsor  Government medical 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 
Dr Indrajit De  Institute of Post Graduate Medical Education and Research  Department of Physical medicine and Rehabilitation OPD and IPD Institute of Postgraduate Medical Education and Research 244 AJC Bose Road, Kolkata- 700020
Kolkata
WEST BENGAL 
8145549644

indrajitde.id@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
IPGME and R Research Oversight Committee  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition: G80||Cerebral palsy,  
 
Intervention / Comparator Agent  
Type  Name  Details 
Intervention  Botulinum Toxin Type A  botulinum toxin type A injections under USG guidance by maintaining proper aseptic condition using 25/27 G needle with max 100 units of inj botulinum toxin type A reconstitute with 2 ml of NS for a single setting with each gland 1U/kg/gland dose with a depth of needle 0.5 to 1 cm. Procedure will be done under local anesthesia and in fasting condition. patient will be followed up after 2 hours of procedure (only for observation), then at 2 weeks, 4 weeks and 12 weeks at outpatient day basis 
Comparator Agent  Oral Glycopyrrolate  glycopyrrolate therapy will be started with a minimum dose of 0.10 mg/kg twice daily dose, after starting medication assessment will be done at 2 weeks,1 month and 3 months interval 
 
Inclusion Criteria  
Age From  4.00 Year(s)
Age To  12.00 Year(s)
Gender  Both 
Details  1.Confirmed case of cerebral palsy.
2.Drooling Severity (DS) Scale score 3 or more.
3.Drooling Frequency (DF) scale score 3 or more.
4.Consent from the guardian or relative 
 
ExclusionCriteria 
Details  1.Local site infection. 2.Allergy to botulinum toxin type A or oral Glycopyrrolate.
3.H/O severe Dysphagia.
4.H/O surgery done for controlling of sialorrhea. Or any h/o of salivary gland excision surgery mainly parotid and submandibular. 5.Abnormal coagulation profile. 6.Patients suffering from unstable cardio vascular or serious respiratory diseases. 
 
Method of Generating Random Sequence   Stratified randomization 
Method of Concealment   Not Applicable 
Blinding/Masking   Open Label 
Primary Outcome  
Outcome  TimePoints 
Ultrasound guided botulinum toxin type A injection to salivary glands (b/l parotid & submandibular) versus otal glycopyrrolate in sialorrhea in cerebral palsy patients will be compared for efficacy  1 year 
 
Secondary Outcome  
Outcome  TimePoints 
Improvement of quality of life physically & psychologically following application of botulinum toxin type A injection over oral glycopyrrolate therapy will be compared.  1 year 
 
Target Sample Size   Total Sample Size="44"
Sample Size from India="44" 
Final Enrollment numbers achieved (Total)= "44"
Final Enrollment numbers achieved (India)="44" 
Phase of Trial   Phase 1/ Phase 2 
Date of First Enrollment (India)   31/07/2023 
Date of Study Completion (India) 13/11/2024 
Date of First Enrollment (Global)  Date Missing 
Date of Study Completion (Global) Date Missing 
Estimated Duration of Trial   Years="1"
Months="6"
Days="0" 
Recruitment Status of Trial (Global)
Modification(s)  
Not Yet Recruiting 
Recruitment Status of Trial (India)  Completed 
Publication Details
Modification(s)  
N/A 
Individual Participant Data (IPD) Sharing Statement

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

Response - NO
Brief Summary
Modification(s)  

Objective of proposed research:

To observe separate efficacy between ultrasound guided botulinum toxin type A injection to salivary glands (parotid and submandibular) and oral Glycopyrrolate therapy for management of sialorrhea in children with cerebral palsy and compare between them.

Background of present study:

 

It is noted in our regular practice that sialorrhea is one of the common presentations in children

with cerebral palsy. Around (15-20%) of physically disabled children are affected by Cerebral Palsy (CP). In India, the estimated incidence is around 3/1000 live births. CP is associated with many comorbidities including sialorrhea. The most common cause of sialorrhea in children is cerebral palsy with an incidence rate of approximate (10 to 58%).

There are a lot of approaches to manage sialorrhea including behavioural interventions, oral and topical medications, radiation therapy and surgery. However, there is currently no satisfactory solution. The use of oral anticholinergic medication like glycopyrrolate is also limited because of several side effects although it has faster onset of action. As sialorrhea is very much difficult to control with this already existing therapy including oral pharmacological therapy. Hence the need for intervention rises.

The application of ultrasound guided botulinum toxin type A injection to salivary glands (parotid and submandibular) has been shown to be a safe and effective option to treat children with moderate and severe sialorrhea, improving quality of life physically and psychologically. But the efficacy of botulinum toxin injection over oral glycopyrrolate is not properly established and very few literatures have been found. with. So, in this study we will aim to clarify whether Botulinum toxin type A injection has additional value over oral glycopyrrolate therapy for management of sialorrhea in cerebral palsy patients.

 

6.      Methodology:

 

 a. Study design: Parallel group, Open label, Randomized Controlled Trial.

 

             b. Study duration: 18 months.                                             

                                                                                                                                                                                                                                                 c. Place of study: Department of Physical Medicine & Rehabilitation (PM&R), IPGME&R and SSKM Hospital, Kolkata.

 

d. Study Population: Patients attending OPDs and admitted in IPDs of Department of PM&R fulfilling inclusion and exclusion criteria.

 

 

e. Sample Size: Total 44(22 in each group).

 

7.   Expected outcome:

Application of ultrasound guided botulinum toxin type A injection to salivary glands (b/l parotid and submandibular) is a better and safe alternative method for management of sialorrhea over existing methods of therapy including oral glycopyrrolate in cerebral palsy patients.

 

 
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