The effect of the implementation a care bundle for the prevention of caesarean wound infection

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20170703034873N3

Enrollment

Registered

2022-10-09

Start date

2022-09-23

Completion date

Unknown

Last updated

2022-11-21

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

Conditions

The effect of the implementation of the care package for the prevention of caesarean section wound infection. Infection of obstetric surgical wound

Interventions

Intervention 1: Intervention group: The recipient of the infection prevention care package will be the operation site, so that pre-surgery care will be provided for patients according to the care pack

Eligibility

Sex/Gender

Female

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Candidates for non-emergency cesarean section due to obstetric and non-obstetric indications Patient consent to participate in the study Being at least 18 years old singleton pregnancy Gestational age greater than or equal to 37 weeks Not suffering from an underlying disease such as severe liver/kidney disorders/diabetes and severe anemia (Hct<33% or Hb<11g/dl) Not using immunosuppressive drugs (cortones) No history of infectious disease and severe malnutrition in the last 6 months The patient's BMI should be less than 35 Failure to detect placenta accreta or placenta previa in ultrasound before caesarean section

Exclusion criteria

Exclusion criteria: Hospitalization for more than 1 week after cesarean section Receiving blood products within the last 10 days Fever above 38 degrees from the time of admission to 48 hours after cesarean section Not being discharged from the first 24 hours after surgery due to the presence of any birth complications Non-referral in the one-month follow-up of the patient

Design outcomes

Primary

Measure	Time frame
Caesarean section wound infection. Timepoint: For patients, pre-surgery care will be provided according to the care package, after the patient is called to the operating room, intra-operative care will be provided, and after the surgery, post-surgery care will be provided in the recovery room and women's surgery department. Method of measurement: Data collection tool The data collection tool in this study is a questionnaire consisting of four sections A: Patient demographic information form B: Patient pregnancy information form C: Patient surgery information form and surgical site infection checklist and REEDA tool will be.	—

Measure

Time frame

Caesarean section wound infection. Timepoint: For patients, pre-surgery care will be provided according to the care package, after the patient is called to the operating room, intra-operative care will be provided, and after the surgery, post-surgery care will be provided in the recovery room and women's surgery department. Method of measurement: Data collection tool The data collection tool in this study is a questionnaire consisting of four sections A: Patient demographic information form B: Patient pregnancy information form C: Patient surgery information form and surgical site infection checklist and REEDA tool will be.

—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFariba Yaghoubinia

Zahedan University of Medical Sciences

yaghoubinia@zaums.ac.ir+98 54 3343 0059

Outcome results

None listed

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