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CTRI Number  CTRI/2025/10/095636 [Registered on: 06/10/2025] Trial Registered Prospectively
Last Modified On: 20/02/2026
Post Graduate Thesis  Yes 
Type of Trial  Interventional 
Type of Study   Drug 
Study Design  Non-randomized, Active Controlled Trial 
Public Title of Study   A study to compare Tramadol and Tapentadol for pain relief in patients after surgery 
Scientific Title of Study   A comparative study between intravenous Tramadol vs intranasal Tapentadol on postoperative analgesia in laparoscopic cholecystectomy. 
Trial Acronym  NIL 
Secondary IDs if Any  
Secondary ID  Identifier 
NIL  NIL 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Dr Sourangshu Biswas 
Designation  Post graduate trainee 
Affiliation  Burdwan Medical College and Hospital 
Address  Dept of Anaesthesiology Burdwan of Medical College

Barddhaman
WEST BENGAL
713104
India 
Phone  6290536601  
Fax    
Email  sourangshu96biswas@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  Dr Tirthasish Mandal 
Designation  Assistant Professor 
Affiliation  Burdwan Medical College and Hospital 
Address  A F2 Aalingan apartment Sanchita Park Bidhannagar P.O.-ABL Durgapur

Barddhaman
WEST BENGAL
713206
India 
Phone  8768726509  
Fax    
Email  tirthasishm@rediffmail.com  
 
Details of Contact Person
Public Query
 
Name  Dr Tirthasish Mandal 
Designation  Assistant Professor 
Affiliation  Burdwan Medical College and Hospital 
Address  A F2 Aalingan apartment Sanchita Park Bidhannagar P.O.-ABL Durgapur

Barddhaman
WEST BENGAL
713206
India 
Phone  8768726509  
Fax    
Email  tirthasishm@rediffmail.com  
 
Source of Monetary or Material Support  
The Principal, Burdwan Medical College and Hospital, P.O.- Baburbag, District- Purba Bardhaman, PIN- 713104, West Bengal, India 
 
Primary Sponsor  
Name  Dr Sourangshu Biswas 
Address  Depart of Anaesthesiology, Office of the Principal, Burdwan Medical College and Hospital, P.O.- Baburbag, District - Purba Bardhaman, PIN- 713104, West Bengal, India 
Type of Sponsor  Other [SELF] 
 
Details of Secondary Sponsor  
Name  Address 
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 Sourangshu Biswas   Burdwan Medical College and Hospital  Department of Anaesthesiology, Office of the Principal, P.O. - Baburbag, District - Purba Bardhaman PIN - 713104
Barddhaman
WEST BENGAL 
6290536601

sourangshu96biswas@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
Burdwan Medical College Institutional Ethics committee   Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition: 3||Administration,  
 
Intervention / Comparator Agent  
Type  Name  Details 
Intervention  Tapentadol hydrochloride  45 mg intrnasally 30 minutes before extubation 
Comparator Agent  Tramadol hydrochloride   1 mg/kg body wt intravenously 30 minutes before extubation 
 
Inclusion Criteria  
Age From  18.00 Year(s)
Age To  60.00 Year(s)
Gender  Both 
Details  ASA I/II patients
undergoing elective cholecystectomy patients
wiling to provide informed consent 
 
ExclusionCriteria 
Details  ASA III or IV
History of bronchial asthma
History of hypersensitivity to the study drugs
Patients having any intranasal pathology
Patients requiring nasal intubation
Serum creatinine more than 2 mg percent
 
 
Method of Generating Random Sequence   Not Applicable 
Method of Concealment   Not Applicable 
Blinding/Masking   Not Applicable 
Primary Outcome  
Outcome  TimePoints 
Pain score on visual analog scale
 
at 0 minute following extubation, at the end of 30th minute, 1st hour,2nd hour,4th hour, 6th hour and 12th hour
in the post operative period 
 
Secondary Outcome  
Outcome  TimePoints 
Sedation score using Ramsay sedation score scale
 
at 0 minute following extubation
at the end of 30th minute
at the end of 1st hour 2nd hour 4th hour 6th hour & 12th hour
in the post operative period 
Nausea & vomiting severity score  at 0 minute following extubation
at the end of 30th minute
at the end of 1st hour 2nd hour 4th hour 6th hour & 12th hour
in the post operative period 
 
Target Sample Size   Total Sample Size="72"
Sample Size from India="72" 
Final Enrollment numbers achieved (Total)= "Applicable only for Completed/Terminated trials"
Final Enrollment numbers achieved (India)="Applicable only for Completed/Terminated trials" 
Phase of Trial   N/A 
Date of First Enrollment (India)   20/10/2025 
Date of Study Completion (India) Applicable only for Completed/Terminated trials 
Date of First Enrollment (Global)  Date Missing 
Date of Study Completion (Global) Applicable only for Completed/Terminated trials 
Estimated Duration of Trial   Years="1"
Months="6"
Days="0" 
Recruitment Status of Trial (Global)
Modification(s)  
Not Applicable 
Recruitment Status of Trial (India)  Open to Recruitment 
Publication Details   N/A 
Individual Participant Data (IPD) Sharing Statement

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

Response - NO
Brief Summary   Acute postoperative pain that is not adequately treated may lead to long-term morbidity. This 
has been the focus of several pharmacotherapies. Considering medication-related adverse 
effects, we wish to compare intravenous (IV) tramadol and intranasal tapentadol in postoperative analgesia following laparoscopic surgery. We evaluated intranasal tapentadol’s 
involvement in post-operative analgesia and its dosage required following laparoscopic 
cholecystectomy, taking into account its improved tolerability profile.

OBJECTIVE:
Primary objective:
The primary objective of our study is to compare postoperative pain severity using visual 
analogue scale (VAS) grading with intranasal tapentadol versus intravenous tramadol in 
patients undergoing elective laparoscopic cholecystectomy under general anaesthesia and 
when the first rescue analgesia given (duration of analgesia).
Secondary objectives:
a. The number of times rescue analgesics are administered in the postoperative period. 
b. Postoperative nausea, vomiting, sedation, and other adverse effects of intranasal 
tapentadol versus intravenous tramadol in patients undergoing elective laparoscopic 
cholecystectomy under general anaesthesia.
METHODOLOGY:
Following ethical approval and informed consent, 72 ASA I-II patients aged 18-60 yrs
scheduled for elective laparoscopic cholecystectomy will be included. They will be separated 
into two groups: Group T will get IV tramadol (1 mg/kg), whereas Group P will receive 
intranasal tapentadol (45 mg) 30 minutes before extubation. Fentanyl, propofol, atracurium, 
glycopyrrolate, midazolam, paracetamol and ondansetron will be used as per standard 
general anaesthesia protocol. Routine post operative analgesia will be provided with infusion 
paracetamol 1 gm IV 12 hourly. The Visual Analogue Scale (VAS) and Ramsay Sedation 
Score (RSS) will evaluate post-operative pain and sedation at 0, ½, 1, 2, 4, 6, and 12 hours, 
respectively. As rescue analgesic injection diclofenac sodium 75 mg IM will be given. Rescue 
analgesic use, adverse effects will all be reported and statistically analysed.
EXPECTED OUTCOME:
A) Because of its rapid mucosal absorption, intranasal tapentadol is likely to provide faster 
onset of analgesia than IV tramadol. 
B) Patients taking intranasal tapentadol may have lower VAS scores, longer durations of 
analgesia, and a lower dose of rescue analgesics. 
C) Tapentadol is believed to have less adverse effects (such as nausea, vomiting, and 
drowsiness), making it more tolerable. Overall, intra nasal tapentadol may prove to be a more 
patient-friendly and efficient alternative to intravenous tramadol for postoperative analgesia in 
laparoscopic cholecystectomy.

 
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