Quality improvement study for the prevention of post caesarean nosocomial infection in a tertiary care centre
Not Applicable
Completed
- Conditions
- Health Condition 1: O758- Other specified complications of labor and delivery
- Registration Number
- CTRI/2023/08/056515
- Lead Sponsor
- Post Graduate Institute of Medical Education and Research Chandigarh
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 253
Inclusion Criteria
patients undergone caesarean section and their caregivers
willing to participate in the study
able to understand Hindi/English/Punjabi
Exclusion Criteria
patients with other gynecological conditions
patients on artificial ventilator
patients not willing to participate in the study
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method to reduce incidence of post caesarean nosocomial infections with in a period of 6 weeks and 8 weeksTimepoint: to reduce incidence of post caesarean nosocomial infections, with in a period of 6 weeks and 8 weeks
- Secondary Outcome Measures
Name Time Method Knowledge & skill of nurses, doctors, other health care workers, patients & care givers regarding the prevention of post caesarean nosocomial infections with in a period of 6 weeks & 8 weeksTimepoint: Knowledge & skill of nurses, doctors, other health care workers, patients & care givers regarding the prevention of post caesarean nosocomial infections with in a period of 6 weeks & 8 weeks