| 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
|
|
|
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. |