Active — Not RecruitingNot Applicable

Wireless Physiologic Monitoring in Postpartum Women

Uganda3,191 participantsStarted 2020-01-21

Plain-language summary

To estimate the clinical effectiveness of wireless physiologic monitoring of women in the first 24 hours after cesarean delivery at Mbarara Regional Referral Hospital

Who can participate

Age range18 Years

SexALL

See this in plain English?

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

Inclusion Criteria: * Emergency cesarean delivery at MRRH * Able to provide consent or have a guardian/attendant present who can consent * Willing to wear the biosensor for 24 hours * Willing remain in the postpartum unit for 24 hours Exclusion Criteria: * Admitted to ICU directly after delivery * Allergies or hypersensitivity to device materials

What they're measuring

Severe Maternal Outcome

Timeframe: From completion of the cesarean delivery until hospital discharge from the procedure, an average of 3 days

Trial details

NCT IDNCT04060667

SponsorMassachusetts General Hospital

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2022-03-30

Results submitted2025-06-03

View on ClinicalTrials.gov More Maternal Death During Childbirth trials