Electronic Monitoring System for Surgical Site Infections
Not Applicable
- Conditions
- Health Condition 1: - Health Condition 2: O- Medical and Surgical
- Registration Number
- CTRI/2018/12/016516
- Lead Sponsor
- Indian Council of Medical Research
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All patients undergoing the surgery and who are willing to participate in the study
Exclusion Criteria
Immunodeficiency patients and patients with prior surgery
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess the prevalence of SSIs <br/ ><br>To determine the pathogens causing SSIs <br/ ><br>To validate the electronic Surveillance SystemTimepoint: During the patient stay in hospital daily monitoring of laboratory reports will be done. <br/ ><br>Post-discharge data will be gathered by telephone and postal questionnaires <br/ ><br>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 Outcome Measures
Name Time Method 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.