FindTrial
Sign In

Electronic Monitoring System for Surgical Site Infections

Development and Validation of an Electronic Surveillance System for Surgical Site Infections developing during hospital stay and after discharge: A Multi-Centric Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2018/12/016516
Enrollment
45000
Registered
2018-12-03
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: - Health Condition 2: O- Medical and Surgical

Interventions

Control Intervention1: NIL: NIL

Sponsors

Indian Council of Medical Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All patients undergoing the surgery and who are willing to participate in the study

Exclusion criteria

Exclusion criteria: Immunodeficiency patients and patients with prior surgery

Design outcomes

Primary

MeasureTime frame
To assess the prevalence of SSIs To determine the pathogens causing SSIs To validate the electronic Surveillance SystemTimepoint: During the patient stay in hospital daily monitoring of laboratory reports will be done. Post-discharge data will be gathered by telephone and postal questionnaires At 30th day (first time), 60 days (second time), 6 months (third time) and 12 months (final follow-up in case of implant surgery) after the operation.—

Secondary

MeasureTime frame
post discharge dataTimepoint: At 30th day (first time), 60 days (second time), 6 months (third time) and 12 months (final follow-up in case of implant surgery) after the operation.—

Countries

India

Contacts

Public ContactDr Chiranjay Mukhopadhyay

Kasturba Medical College

chranjay.m@manipal.edu9845513057

Outcome results

None listed

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