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Efficacy of Using a Closing Pack to Reduce Postpartum Sepsis

NCT05632705 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1000

Last updated 2022-11-30

No results posted yet for this study

Summary

Randomised trial comparing the efficacy and feasibility of using a sterile closing pack to reduce postpartum sepsis

Conditions

  • Prevention of Postpartum Sepsis

Interventions

OTHER

Closing pack

A closing pack, new sterile gloves and new sterile drapes will be used when commencing closure of the sheath and skin

Sponsors & Collaborators

  • University of Pretoria

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-03-08
Primary Completion
2022-01-31
Completion
2022-04-30

Countries

  • South Africa

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05632705 on ClinicalTrials.gov