| CTRI Number |
CTRI/2025/09/095416 [Registered on: 26/09/2025] Trial Registered Prospectively |
| Last Modified On: |
26/09/2025 |
| Post Graduate Thesis |
Yes |
| Type of Trial |
Interventional |
|
Type of Study
|
Drug |
| Study Design |
Randomized, Parallel Group Trial |
|
Public Title of Study
|
ComparingVitamin B6 Plus Ondanetron Versus Ondansetron Alone to Prevent Nausea and Vomiting In Laproscopic Surgery: A Doulbe-Blind Study |
|
Scientific Title of Study
|
Comparison of Pyridoxine-Ondansetron Versus Ondansetron alone for post Operative Nausea Vomiting Prophylaxis in Laprroscopic Surgery: A Randomised Double Blind Trial |
| 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 Sakshi |
| Designation |
Post graduate student |
| Affiliation |
University College of Medical Sciences and GTB Hospital,Delhi |
| Address |
2nd floor, Ot Block,Department of Anesthesiology and Critical care,UCMS and GTB Hospital, Delhi
New Delhi DELHI 110093 India |
| Phone |
8684097975 |
| Fax |
|
| Email |
sakshigarg623@gmail.com |
|
Details of Contact Person Scientific Query
|
| Name |
Dr Rashmi Salhotra |
| Designation |
Professor |
| Affiliation |
University College of Medical Sciences and GTB Hospital, Delhi |
| Address |
631B, 6th floor, Ot Block, Department of Anesthesiology and Critical Care, UCMS and GTB Hospital, Delhi
New Delhi DELHI 110093 India |
| Phone |
9911317334 |
| Fax |
|
| Email |
rsalhotra@ucms.ac.in |
|
Details of Contact Person Public Query
|
| Name |
Dr Sakshi |
| Designation |
Post graduate student |
| Affiliation |
University College of Medical Sciences and GTB Hospital |
| Address |
2nd floor, Ot Block, Department of Anesthesiology and Critical care, UCMS and GTB Hospital, Delhi
New Delhi DELHI 110093 India |
| Phone |
8684097975 |
| Fax |
|
| Email |
sakshigarg623@gmail.com |
|
|
Source of Monetary or Material Support
|
| UCMS and GTB HOSPITAL, DELHI, 110093, INDIA |
|
|
Primary Sponsor
|
| Name |
UCMS and GTB Hospital |
| Address |
GTB Hospital, Dilshad Garden, New Delhi, 110093, INDIA |
| 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 Sakshi |
University College of Medical Sciences and GTB Hospital |
Department of Anesthesiology and Critical Care, 2nd floor, Ot Block, GTB hospital, Dilshad Garden, 110093, India, east delhi East DELHI |
8684097975
sakshigarg623@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 will be given preoperatively |
1 h before surgery |
| Comparator Agent |
Group NO |
No drug will be given preoperatively |
| Comparator Agent |
Oral pyridoxine tablet |
1 h prior to surgery in group PO |
|
|
Inclusion Criteria
|
| Age From |
18.00 Year(s) |
| Age To |
99.00 Year(s) |
| Gender |
Female |
| Details |
Consenting ASAI/II
adult females
Undergoing laparoscopic surgery
Requiring general anesthesia |
|
| ExclusionCriteria |
| Details |
Pregnant patient,
Patient with cardiac, hepatic and renal disease and known case of tuberculosis
Developmental delay, mental illness, severe neurological disease
Allergic to any drug used in study
Long term use of long-acting antiemetic, emetogenic drugs, opoids, glucocorticoids or cancer therapy and add on any antiemetic in last 24 hours |
|
|
Method of Generating Random Sequence
|
Computer generated randomization |
|
Method of Concealment
|
Sequentially numbered, sealed, opaque envelopes |
|
Blinding/Masking
|
Participant, Investigator and Outcome Assessor Blinded |
|
Primary Outcome
|
| Outcome |
TimePoints |
| Incidence of post operative nausea vomiting(PONV) in first 24 hour after surgery |
Postoperative-
0-2 hour, 2-6 hour, 6-12 hour, 12-24 hour |
|
|
Secondary Outcome
|
| Outcome |
TimePoints |
Time to first occurrence of PONV
Severity of PONV
Requirement of rescue antiemetic drugs
Side effects, if any |
Intraoperative-
15 min, 30 min, 60min, 90 min, 120 min, 150 min, 180 min, 210 min
Postoperative-
0-2 hour, 2-6 hour, 6-12 hour, 12-24hour |
|
|
Target Sample Size
|
Total Sample Size="90" Sample Size from India="90"
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
|
Post Marketing Surveillance |
|
Date of First Enrollment (India)
|
15/10/2025 |
| 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="5" Days="0" |
|
Recruitment Status of Trial (Global)
|
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
|
Title: Comparison of Pyridoxine-Ondansetron Versus Ondansetron alone for Postoperative Nausea Vomiting Prophylaxis in Laparoscopic Surgery: A Randomised Double Blind Trial Rationale: Post-operative nausea vomiting (PONV) is a common and distressing complication of anesthesia and the frequency increases with increase in the number of risk factors. Therefore, prophylaxis of PONV with at least two drugs is advised. Ondansetron with other antiemetic forms a good prophylactic combination for PONV however, the efficiency of Ondansetron with pyridoxine (commonly used drug for hyperemesis gravidarum) for PONV prophylaxis has not been established so far. Aim: To compare pyridoxine-Ondansetron versus Ondansetron alone for post operative nausea vomiting prophylaxis in laparoscopic surgery. Objective: To compare pyridoxine-Ondansetron versus Ondansetron alone for post operative nausea vomiting prophylaxis in laparoscopic surgery. Primary objective: Incidence of PONV in first 24 hours after surgery. Secondary objective: 1. Severity of PONV 2. Requirements of rescue antiemetic drugs. 3. Side effects , if any Methods: This prospective, randomised double blind study will be conducted after obtaining Ethical committee approval and written informed consent from July 2025-December 2026 in the Department of Anesthesiology and Critical Care, UCMS and GTB Hospital, Delhi. Inclusion criteria: Consenting ASAI/II, adult females >= 18 years old undergoing laparoscopy surgery requiring general anesthesia. Exclusion criteria: 1. Pregnant patients 2. Patients with cardiac, hepatic, renal disease and k/c/o tuberculosis. 3. Developmental delay, mental illness, severe neurological disease. 4. Allergic to any drug used in study. 5. Long term use of long acting antiemetics, emetogenic drugs, opoids, glucocorticoids or cancer chemotherapy and on any antiemetic in last 24 hours. Tablet pyridoxine 200 mg will be given 60 minutes before induction of anesthesia with 1-2 sips of water in one of the 2 groups of patients. After evaluating the risk factors on Koivuranta score, monitors will be attached. General anesthesia will be induced with fentanyl (2mcg/kg)i.v. , propofol (2mg/kg) i.v and vecuronium (0.1mg/ kg) i.v. Endotracheal intubation will be done and anesthesia will be maintained with isoflurane1-1.5% in air and oxygen. Ondansetron 4mg i.v. and paracetamol 1gm i.v. will be given 30 minutes before the end of surgery. Neuromuscular block will be reversed with neostigmine (0.05mg/kg) i.v. and glycopyollate (0.01 mg /kg)i.v. at the end of surgery and trachea will be extubated. If the patient develop nausea lasting >15 min or vomiting in the prospective period, Metoclopramide (rescue antiemetic) 10 mg i.v. will be given slowly. If PONV persist despite administering rescue antiemetic, the physician will be allowed to give additional antiemetics as per discretion. Outcome measures: Incidence of PONV , time to first occurrence of PONV, severity, requirement of rescue antiemetic and side effects, if any, will be recorded until 24 hours post surgery. Sample size calculation: as per previous study, PONV incidence was found was found to be 28% with Ondansetron alone and 6% when combination of Ondansetron- dexamethasone was given, i.e an absolute reduction by 22%. In the absence of incidence for Ondansetron- pyridoxine combination, to estimate an absolute risk reduction in the incidence of PONV by 22%, 41 patients in each group is required at alpha error of 5% and power of 80%, i.e. minimum of 82 patients. To account for 10% loss to follow up , 90 patients will be included with 45 in each group. STATISTICAL ANALYSIS: Statistical analysis will be done in SPS. Patient will be analysed based on intention to treat trial. Normality of data will be tested using kolmogrov-Smirnov test. Quantitative variables will be reported as mean+- SD or median [IQR] depending upon their distribution as normal or non normal respectively, and qualitative variables will be reported as number(percentage). Unpaired t-test and Maan-Whitney U test will be used for analysis of qualitative variables. Repeated measures ANOVA will be used for analysis of repeatedly measured parameters. P<0.05 will be considered significant.
|