TerminatedPhase 2

Non Surgical Management for Uterine Residua After Pregnancy Termination, Abortion or Delivery

Stopped: The principal investigator left the organization

Israel23 participantsStarted 2010-06

Plain-language summary

The aim of the study is to find out whether conservative treatment - expectant management or medical therapy using misoprostol is beneficial in the case of uterine residua, and which treatment is better.

Who can participate

Age range18 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: * women with sonographic examination reveals suspicion of intra-uterine residua after completion of pregnancy * intrauterine cavity, including endometrium, will be at least 15mm Exclusion Criteria: * the need for emergency surgical treatment (curettage) * fever - at least 38 celsius degree * women who had medical termination of pregnancy and the examination is after less then 2 weeks since treatment

What they're measuring

abscence of sonographic finding in the uterine cavity

Timeframe: one week since recruitment

Trial details

NCT IDNCT01134926

SponsorHaEmek Medical Center, Israel

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2012-05

View on ClinicalTrials.gov More Intra-uterine Residua trials