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CTRI Number  CTRI/2025/04/084592 [Registered on: 11/04/2025] Trial Registered Prospectively
Last Modified On: 16/03/2026
Post Graduate Thesis  No 
Type of Trial  Interventional 
Type of Study   Preventive
Behavioral 
Study Design  Cluster Randomized Trial 
Public Title of Study   Approaches to Reducing Infections after surgery and Improving Patient Outcomes" 
Scientific Title of Study   A multimodal, adaptive, intervention to prevent perioperative infection and reduce mortality: a stepped-wedge cluster RCT (The Modified Clean Cut 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 Amit Mahajan  
Designation  Professor 
Affiliation  Christian Medical College & Hospital Ludhiana 
Address  Department of General Surgery, First Floor 1138

Ludhiana
PUNJAB
141008
India 
Phone  9988018700  
Fax    
Email  dr_amitrock@yahoo.co.in  
 
Details of Contact Person
Scientific Query
 
Name  Dr Dhruva Ghosh 
Designation  Professor 
Affiliation  Christian Medical College & Hospital Ludhiana  
Address  Department Of Paediatric Surgery

Ludhiana
PUNJAB
141008
India 
Phone  9915198894  
Fax    
Email  dhruvghosh73@gmail.com  
 
Details of Contact Person
Public Query
 
Name  Dr Dhruva Ghosh 
Designation  Professor 
Affiliation  Christian Medical College & Hospital Ludhiana  
Address  Department Of Paediatric Surgery

Ludhiana
PUNJAB
141008
India 
Phone  9915198894  
Fax    
Email  dhruvghosh73@gmail.com  
 
Source of Monetary or Material Support  
Indian Council of Medical Research Department of Health Research Ministry of Health & Family Welfare Government of India Ansari Nagar, New Delhi - 110029, India www.icmr.gov.in  
 
Primary Sponsor  
Name  Indian Council of Medical Research New Delhi  
Address  Indian Council of Medical Research Department of Health Research Ministry of Health & Family Welfare Government of India Ansari Nagar New Delhi 110029 India www.icmr.gov.in 
Type of Sponsor  Research institution 
 
Details of Secondary Sponsor  
Name  Address 
Christian Medical College Hospital Ludhiana   Christian Medical College Hospital Ludhiana Brown Road 141008 Punjab India globalsurgindia@cmcludhiana.in 1612115152 
 
Countries of Recruitment     India  
Sites of Study  
No of Sites = 10  
Name of Principal Investigator  Name of Site  Site Address  Phone/Fax/Email 
Dr Reshma Ambulkar   ACTREC, Tata Memorial Hospital  Department of Anesthesiology, Critical Care and Pain, 248 Paymaster Shodika
Mumbai
MAHARASHTRA 
9821790448

rambulkar@hotmail.com 
Dr Anju Grewal   All India Institute of Medical Sciences  Department of Anesthesiology
Bathinda
PUNJAB 
9815482626

dranjugrewal@gmail.com 
Dr Kirti Kumar J Rathod  All India Institute of Medical Sciences  Department Of Paediatric Surgery
Jodhpur
RAJASTHAN 
8769429995

drkirtirathod@gmail.com 
Dr Nitu Mishra   All India Institute of Medical Sciences   Department of Obstetrics and Gynecology
Bhopal
MADHYA PRADESH 
9592365444

nitumishra07@gmail.com 
Dr Vijay Kundal   All India Institute of Medical Sciences  Department of Pediatric Surgery
Jammu
JAMMU & KASHMIR 
9910939123

vijay.kumar@aiimsjammu.edu.in 
Dr Amit Mahajan  Christian Medical College Hospital  Department of General Surgery, First Floor room number 1138
Ludhiana
PUNJAB 
9988018700

dr_amitrock@yahoo.co.in 
Dr AK Attri   Government Medical College   Department of Surgery,B-block, Level III Room no D347
Chandigarh
CHANDIGARH 
9646121561

attriak@yahoo.com  
Dr Raman Katariya   Jan Swasthya Sahyog Hospital  Department of Pediatric Surgery
Bilaspur
CHHATTISGARH 
9589402995

k.drraman@gmail.com 
Dr Arpit Mathew  Madhepura Christian Hospital  Department of Surgery
Madhepura
BIHAR 
9888922600

arpitmathew@eha-health.org 
DrJacob Jayakar  Pondicherry Institute of Medical Sciences Kalapet  Department of General Surgery
Pondicherry
PONDICHERRY 
96556 97457

generalsurgerypims@gmail.com 
 
Details of Ethics Committee
Modification(s)  
No of Ethics Committees= 10  
Name of Committee  Approval Status 
Institutional Ethics Committee   Submittted/Under Review 
Institutional Ethics Committee   Approved 
Institutional Ethics Committee AIIMS Bathinda   Approved 
Institutional Ethics Committee AIIMS Bhopal   Approved 
Institutional Ethics Committee AIIMS Jammu  Approved 
Institutional Ethics Committee AIIMS Jodhpur   Approved 
Institutional Ethics Committee CMC Ludhiana   Approved 
Institutional Ethics Committee GMC Chandigarh  Approved 
Institutional Ethics Committee JSS  Approved 
Institutional Ethics Committee Pondicherry Institute of Medical Sciences  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition: Y839||Surgical procedure, unspecified asthe cause of abnormal reaction of the patient, or of later complication, without mention of misadventure at the time of the procedure, (2) ICD-10 Condition: N998||Other intraoperative and postprocedural complications and disorders of genitourinary system, (3) ICD-10 Condition: K918||Other intraoperative and postprocedural complications and disorders of digestive system, (4) ICD-10 Condition: O94-O9A||Other obstetric conditions, not elsewhere classified,  
 
Intervention / Comparator Agent  
Type  Name  Details 
Intervention  Modified Clean Cut Intervention  Adherence to seven critical standards of perioperative infection prevention and control: 1. Appropriate skin preparation of both the surgeon’s hands and the surgical site with proper antiseptic agents 2. Maintenance of the sterile field by ensuring the integrity and sterility of surgical gowns, drapes, and gloves. 3. Appropriate antibiotic selection and administration, when indicated, within one hour prior to surgical incision to optimise prophylaxis 4. Proper confirmation of instrument sterility by the operating team 5. Complete gauze/swab counts every case at appropriate times (preoperatively, before organ space and/or cavity closure, and postoperatively) 6. Change of Gloves and Instruments by the Surgical Team at the time of Fascial Closure in Contaminated and Dirty Abdominal Operations. 7. Use of the Surgical Safety Checklist to promote teamwork, communication, and a culture of safety in the operating room  
Comparator Agent  Normal Practice  Normal practice prior to Modified Clean Cut Intervention and training for same 
 
Inclusion Criteria  
Age From  0.00 Day(s)
Age To  99.00 Year(s)
Gender  Both 
Details  1. Patient undergoing any abdominal surgery (including the abdominal wall or entering the abdominal or retroperitoneal cavities)
2. Any age, gender of patient
3. Ability to complete postoperative 30 day follow up

 
 
ExclusionCriteria 
Details  1. Surgery in any part of the body other than abdomen
2. Patient unable to complete postoperative 30 day follow-up.
 
 
Method of Generating Random Sequence   Computer generated randomization 
Method of Concealment   Not Applicable 
Blinding/Masking   Not Applicable 
Primary Outcome  
Outcome  TimePoints 
Primary outcomes include Surgical Site Infections (SSIs) up to 30 days
of surgery 
Primary outcomes include Surgical Site Infections (SSIs) up to 30 days
of surgery 
 
Secondary Outcome  
Outcome  TimePoints 
Secondary outcomes include all cause mortality , length of stay, reoperation for any reason
(planned or unplanned), and overall compliance with the seven perioperative infection
prevention standards during the intervention period. 
30day follow up  
 
Target Sample Size   Total Sample Size="980"
Sample Size from India="980" 
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)   01/05/2025 
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="3"
Months="0"
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  
A multimodal, adaptive, intervention to prevent perioperative infection and reduce mortality: a
stepped-wedge cluster RCT (The Modified Clean Cut Trial)

The purpose of Clean Cut is to:
(1) help facilitate improved adherence to critical perioperative infection prevention practices
and lower surgical site infection rates; postoperative morbidity and mortality.
(2) create an environment conducive to successful implementation of the WHO Surgical Safety
Checklist;
(3) foster a culture of teamwork, individual value, and accountability that facilitates quality
improvement more broadly.

Research questions: Does a surgical infection prevention programme intervention lead to a reduction in surgical infections and postoperative mortality? Can we increase adherence to critical standards of perioperative care in a sustainable manner?
What are the barriers and facilitators to compliance with perioperative standards? Is a strategy of peer-to-peer learning and hub-and-spoke support adequate for effective implementation?

Study design and sample size: Stepped wedge, mixed methods, team-based intervention to improve compliance with seven critical perioperative infection prevention standards in 900 patients undergoing abdominal surgery.

Intervention: Clean Cut has been developed through a collaboration informed and led by
LMIC healthcare staff. Further modifications to this intervention have been added to this by the India Hub of the NIHR Health Research Unit On Global Surgery following our work especially in the Cheetah Trial. It involves a sequential intervention to address problems in adhering to seven critical standards of perioperative infection prevention and control:
1) Appropriate skin preparation of both the surgeon’s hands and the surgical site with proper
antiseptic agents
2) Maintenance of the sterile field by ensuring the integrity and sterility of surgical gowns,
drapes, and gloves.
3) Appropriate antibiotic selection and administration, when indicated, within one hour prior
to surgical incision to optimise prophylaxis
4) Proper confirmation of instrument sterility by the operating team
5) Complete gauze/swab counts every case at appropriate times (preoperatively, before organ
space and/or cavity closure, and postoperatively)
6) Change of Gloves and Instruments by the Surgical Team at the time of Fascial Closure in
Contaminated and Dirty Abdominal Operations.
7) Use of the Surgical Safety Checklist to promote teamwork, communication, and a culture
of safety in the operating room

The qualitative part of the study will involve a validated patient safety questionnaire administered to perioperative personnel and surgeons. A semi structured interview and focussed group discussions will also be conducted to identify barriers to teamwork and patient safety in the operating room and find solutions.
Duration: 36 months

Statistical Analysis Plan: Key variables including compliance with perioperative standards and
patient outcomes will be measured using standardized tools and assessments. Data will be
collected using electronic data capture systems and analyzed using appropriate statistical
methods, including regression analysis to evaluate the intervention’s impact on primary and
secondary outcomes. Data will be summarized using frequency distribution and descriptive
analysis. The normality of the data will be assessed through the statistical test and graphical
method. The p-value of 0.05 will be considered as statistically significant. Summary statistics
will be presented for all outcome measures, with the relevant adjusted effect measures, 95%
confidence intervals and p-values from two-sided tests. The adjusted model will include hospital
as fixed effects and centre as a random effect to account for the clustered nature of the sample.
Quantitative data will be analyzed using statistical software such as R or SPSS, while qualitative
data will be analyzed thematically.
 
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