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EFFECTIVENESS OF PREOPERATIVE VAGINAL CLEANING IN REDUCING POST CAESAREAN INFECTIOUS MORBIDITY

EFFECTIVENESS OF PREOPERATIVE VAGINAL CLEANING IN REDUCING POST CAESAREAN INFECTIOUS MORBIDITY

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07053995
Enrollment
76
Registered
2025-07-08
Start date
2021-02-01
Completion date
2021-07-31
Last updated
2025-07-08

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

Conditions

Endometrial, Infection, Surgical Site Infection Following Cesarean Delivery

Brief summary

After obtaining an informed consent a detailed history and clinical examination was performed. Labs were carried out to fulfill inclusion and exclusion criteria. Women were randomly divided into two groups. In Intervention group vaginal cleaning was done with 50cc diluted antiseptic solution where as control group had abdominal scrub only. Participants were followed and incision site was checked at day 14.

Detailed description

After obtaining an informed consent a detailed history and clinical examination was performed. Labs were carried out to fulfill inclusion and exclusion criteria. Women were randomly divided into two groups. In Intervention group vaginal cleaning was done with 50cc diluted antiseptic solution as single push where as control group had abdominal scrub only. Participants were followed and incision site was checked at day 14. Data was recorded and analyzed.

Interventions

PROCEDUREVaginal cleaning

Before giving incision for C-section surgery, vaginal cleaning was done with 50cc diluted antiseptic solution as a single push.

OTHERNon vaginal cleansing

Routine abdominal scrubbing was carried out before incision. No vaginal cleaning was done before incision.

Sponsors

Khyber Teaching Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* Pregnant women between 18-40 years * Gestational age greater than 36 weeks undergoing elective C section

Exclusion criteria

* Pregnant women with history of allergic reactions to chlorhexidine * Placenta previa on ultrasound scan * Diabetes Mellitus on fasting blood sugar * Anemia (Hb less than 7g/dl)

Design outcomes

Primary

MeasureTime frameDescription
Endometrial Infection14 daysBody temperature was measured postoperatively along with any dicharge of pain around uterine region 24hrs after surgery
Surgical site infection14 daysIncision site was inspected on 4th and 14th post operative day and documented any evidence of infection signs according to Southampton wound grading system.

Countries

Pakistan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026