Clinical Trials Directory

Trials / Terminated

TerminatedNCT01134926

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

Phase Study Comparing Between Expectant Management and Misoprostol Treatment for Intra-uterine Residua After Pregnancy Termination, Abortion or Delivery

Status
Terminated
Phase
Phase 2
Study type
Interventional
Enrollment
23 (actual)
Sponsor
HaEmek Medical Center, Israel · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

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.

Detailed description

Retained products of conception are estimated to occur after approximately 1-6% of pregnancies, probably more often after termination of early pregnancies then after term pregnancy. Complication are abdominal pain, infection, bleeding and for the long term - intrauterine adhesions.Blood clots in the uterine cavity can cause similar complications. The definitive treatment is curettage or hysteroscopy, both of which are carried out under general anesthesia and require an operating theater. Although expectant management and uterotonic drugs are practically used in such situation, they are not described in the literature.This study compare between the outcome of misoprostol treatment and expectant management in the case of intrauterine residua after completion of pregnancy.

Conditions

Interventions

TypeNameDescription
DRUGmisoprostol8oo mcg intravaginal, second dose after one day if there is no response

Timeline

Start date
2010-06-01
Primary completion
2012-05-01
Completion
2012-05-01
First posted
2010-06-02
Last updated
2015-06-23

Locations

1 site across 1 country: Israel

Source: ClinicalTrials.gov record NCT01134926. Inclusion in this directory is not an endorsement.