| 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
|
|
|
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
|
|
|
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
|
|
|
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 - Total requirement of rescue antiemetic in the first 24 hr
- 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 - Total requirement of rescue antiemetic in the first 24 hr
- 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. |