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CTRI Number  CTRI/2025/10/095654 [Registered on: 06/10/2025] Trial Registered Prospectively
Last Modified On: 02/01/2026
Post Graduate Thesis  Yes 
Type of Trial  Interventional 
Type of Study   Drug 
Study Design  Randomized, Parallel Group, Active Controlled Trial 
Public Title of Study   Two drug combination vs one drug for prevention of vomiting after operation 
Scientific Title of Study   Comparison of ondansetron-olanzapine combination with ondansetron alone for PONV prophylaxis in patients scheduled for laparoscopic cholecystectomy: A Randomized Controlled Study 
Trial Acronym  NIL 
Secondary IDs if Any  
Secondary ID  Identifier 
NIL  NIL 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Himani 
Designation  PG Student 
Affiliation  UCMS and GTB Hospital 
Address  Department of Anaesthesiology, UCMS and GTB Hospital

North East
DELHI
110095
India 
Phone  9818613288  
Fax    
Email  drhimanigarg01@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  RS rautela 
Designation  Director professor 
Affiliation  UCMS and GTB Hospital 
Address  Department of Anaesthesiology, UCMS and GTB Hospital

North East
DELHI
110095
India 
Phone  9868399699  
Fax    
Email  rsramb@yahoo.co.in  
 
Details of Contact Person
Public Query
 
Name  Himani 
Designation  PG student 
Affiliation  UCMS and GTB Hospital 
Address  Department of Anaesthesiology, UCMS and GTB Hospital

North East
DELHI
110095
India 
Phone  9818613288  
Fax    
Email  drhimanigarg01@gmail.com  
 
Source of Monetary or Material Support  
NIL 
 
Primary Sponsor  
Name  University college of medical sciences 
Address  Room No 631 B Guru Teg Bahadur Hospital, Dilshad Garden, Delhi 110095 
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 Himani Garg  GTB Hospital  Room No 231 B Department of Anaesthesiology, UCMS and GTB Hospital, Dilshad garden
North East
DELHI 
9818613288

drhimanigarg01@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
Institutional Ethics Committee-Human Research (IEC-HR)   Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition: O||Medical and Surgical,  
 
Intervention / Comparator Agent  
Type  Name  Details 
Intervention  Antiemetic agent will be given  Drug will be given once, 2 h before anaesthesia and 30 min before extubation 
Comparator Agent  olanzapine-ondansetron combination  Each drug will be given only once Olanzepine 200 mg orally 2h before anaesthesia induction Ondansetron 4 mg intravenous 30 min before extubation 
Comparator Agent  Ondansetron 4 mg intravenous  Drug will be given once 30 min before extubation 
 
Inclusion Criteria  
Age From  18.00 Year(s)
Age To  99.00 Year(s)
Gender  Both 
Details  ASA physical status I or II, undergoing laparoscopic cholecystectomy for gall stone disease under GA 
 
ExclusionCriteria 
Details  .Pregnant patients
.Patients having cardiac, hepatic or renal disease
.Patients with history of psychiatric disorder or currently on olanzapine
.Allergic to any drug used in study
.Long term use of long acting antiemetics, emetogenic drugs, opioids, glucocorticoids or cancer chemotherapy.
 
 
Method of Generating Random Sequence   Computer generated randomization 
Method of Concealment   Sequentially numbered, sealed, opaque envelopes 
Blinding/Masking   Not Applicable 
Primary Outcome  
Outcome  TimePoints 
Incidence of PONV in the initial 24 hrs after surgery  Incidence of PONV in the initial 24 hrs after surgery 
 
Secondary Outcome  
Outcome  TimePoints 
1.Severity of PONV in the first 24 hr
2.Total requirement of rescue antiemetic in the first 24 hr
 
0-2hrs, 2-6hrs, 6-12hrs, 12-24hrs 
 
Target Sample Size   Total Sample Size="102"
Sample Size from India="102" 
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)   30/10/2025 
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="4"
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  

Study Title: Comparison of ondansetron-olanzapine combination with ondansetron alone for PONV prophylaxis in patients scheduled for laparoscopic cholecystectomy: A Randomized Controlled Study

 

 Rationale: Post operative nausea and vomiting is a distressing complication following surgery. The incidence of PONV is as high 50-70% in laparoscopic cholecystectomy surgeries. Ondansetron 4mg iv has been used to prevent PONV after laparoscopic cholecystectomies, but in 22% patients, PONV is still seen even after use of ondansetron. Olanzapine has been used to prevent and treat nausea and vomiting in patients undergoing chemotherapy. Moreover, synergism is a known phenomenon when a combination of drugs is used. Review of literature did not reveal any study comparing the efficacy of combination of ondansetron and olanzapine with ondansetron alone for PONV prophylaxis in laparoscopic cholecystectomy surgeries.

AIM: To compare the efficacy of ondansetron-olanzapine combination with ondansetron alone for PONV prophylaxis in patients scheduled for laparoscopic cholecystectomy

OBJECTIVES: To compare the efficacy of ondansetron-olanzapine combination with ondansetron alone for PONV prophylaxis in terms of:

Primary:

     Incidence of PONV in the initial 24 hrs after surgery

Secondary:

1.     Severity of PONV in the first 24 hr

  1. Total requirement of rescue antiemetic in the first 24 hr
  2. Incidence of drug-related side effects, if any.

Materials and method

SETTING: Department of Anaesthesiology and Critical Care

UCMS & G.T.B. Hospital, Delhi-95

Study design: Randomized Double - Blind study

Time frame: August 2025 – November 2026

 

Participants:

Inclusion Criteria:

·       Patients aged >18 years, with ASA physical status I or II, undergoing laproscopic cholecystectomy for gallstone disease under GA

Exclusion Criteria :

·       Pregnant patients

·       Patients with cardiac, hepatic and renal disease

·       Patients with history of psychiatric disorder or currently on olanzapine.

·       Allergic to any drug used in study

·       Long term use of long acting antiemetics, emetogenic drugs, opioids, glucocorticoids or cancer chemotherapy.

Primary outcome

      Incidence of PONV in the initial 24 hrs after surgery

Secondary outcome

1.     Severity of PONV in the first 24 hr

  1. Total requirement of rescue antiemetic in the first 24 hr
  2. Incidence of drug-related side effects, if any

ALLOCATION

Patients will be randomly allocated into:

Group T (n=51) – Patients will receive Olanzapine 5 mg orally (2 hrs before surgery) and Ondansetron 4 mg i.v (given near the end of surgery)

Group C (n=51)- Patients will receive Ondansetron 4mg i.v. (given near the end of the surgery)

Randomization will be done using computer-generated random number tables. The allocation concealment will be done using sequentially numbered opaque-coloured sealed envelopes. The study drug will be prepared by the third person not involved in the study.

Statistical analysis:

Categorical variables will be compared using the chi-square test or fisher’s exact test. Continuous variables will be compared using independent t-test. P- value less than 0.05 will be considered statistically significant.


 

 
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