CompletedNot Applicable

Efficacy of Using a Closing Pack to Reduce Postpartum Sepsis

South Africa1,000 participantsStarted 2021-03-08

Plain-language summary

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

Who can participate

Age range18 Years

SexFEMALE

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * women 18 years and older willing and able to provide consent Exclusion Criteria: * women who are not able or willing to provide consent patients with existing maternal infection

What they're measuring

Efficacy to reduce surgical site infections within seven days

Timeframe: Seven days post-operatively

Trial details

NCT IDNCT05632705

SponsorUniversity of Pretoria

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2022-01-31

View on ClinicalTrials.gov More Prevention of Postpartum Sepsis trials