CompletedPhase 4

The Effect of Rectal and Sublingual Misoprostol Administration in Postpartum or Intrapartum Haemorrhage at Elective Caesarean Delivery: a Randomized Controlled Trial

618 participantsStarted 2013-06

Plain-language summary

The investigators hypothesis in this study is that administration of rectal and sublingual misoprostol decreases intrapartum and postpartum haemorrhage.

Who can participate

Age range18 Years – 44 Years

SexFEMALE

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

✓. live and singleton pregnancy
✓. Elective caesarean
✓. Gestational week greater than 37 weeks
✓. patient between 18-44 year old

Exclusion criteria

✕. -multiple pregnancy
✕. Preeclampsia
✕. Gestational diabetes
✕. Macrosomia
✕. Oligohidraamnıos
✕. Polihidraamnıos
✕. Myoma
✕. Morbid obesity

What they're measuring

Postpartum Haemorrhage

Timeframe: postpartum 24 hour

Trial details

NCT IDNCT01931410

SponsorIstanbul Bakirkoy Maternity and Children Diseases Hospital

Sponsor typeOTHER_GOV

Study typeINTERVENTIONAL

Primary completion2014-01

View on ClinicalTrials.gov More ıntrapartum Haemorrhage trials