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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  
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 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  
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 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.




 
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