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Is there a difference in outcome of patients undergoing surgery after recovery from COVID 19. A multicentre study in India.

A national multi-centre observational case control study on the 30-day morbidity and mortality of abdominal surgical procedures in patients recovered from SARS CoV-2 infection: IAGES Collaborative Study - COVIDIAGES

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2021/01/030794
Enrollment
442
Registered
2021-01-28
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: B972- Coronavirus as the cause of diseases classified elsewhere Health Condition 2: B338- Other specified viral diseases

Interventions

Control Intervention1: NIL: NIL

Sponsors

IAGES Indian Association of GastroEndoscopic Surgeons
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Abdominal surgical procedures including colorectal surgery, general surgery, hepatobiliary surgery, oesophagogastric surgery, transplant surgery, trauma surgery and abdominal vascular surgery. Day care surgery and inpatient surgery are included. All consecutive patients, more than or equal to 18 years , operated from the date of study initiation need to included regardless of emergency or elective status, major or minor status , minimal invasive or open status , day care or indoor admission status , and, irrespective of the seniority of the operating surgeon. All the patients have to mandatorily have the immediate pre-op (within 72 hours) RT PCR Swab test for SARS CoV-2 infection. All patients undergoing abdominal surgery in an operation theatre regardless of the mode of anaesthesia â?? General, Spinal, Epidural, Regional, or Local.

Exclusion criteria

Exclusion criteria: EXCLUSION CRITERIA FOR PATIENTS: All patients Patients undergoing gynaecological or urological procedures. Patients undergoing procedures outside of an operation theatre setting. Patients undergoing an emergency operation with undetermined SARS CoV-2 infection exposure status preoperatively, but test results determined post operatively establish the infected status (postoperative RT PCR swab test positive).

Design outcomes

Primary

MeasureTime frame
To determine the 30-day morbidity and mortality of in those patients who were previously exposed to SARS CoV-2 infection and nare now undergoing major abdominal surgery in India. Timepoint: 30 days—

Secondary

MeasureTime frame
30-day extra pulmonary morbidity Monitor the impact of markers indicating the severity of SARS CoV-2 infection on surgical outcome. To identify the safe duration after resolution of clinical SARS CoV-2 infection when surgery can be undertaken without any added risk of adverse outcomes owing to the previous SARS CoV-2 infection. To determine the predictive factors for complications in such patientsTimepoint: 30 days—

Countries

India

Contacts

Public Contactpankaj bansal

Santokba DurlabhJi Memorial Hospital

bhojwani@docsindia.in9829176755

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026