Treatment of Late Abortion: Evacuatio Uteri or Conservative Treatment
May 31, 2006 updated by: Rigshospitalet, Denmark
Evacuatio Uteri or Conservtive Treatment After Late Abortion. A Randomize Trial.
A randomize trial: expectation or evacuatio uteri for the treatment after late abortion
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Detailed Description
A randomize trial adressing 200 women consecutively recruited from clinical practice at Rigshospitalet.Expectation: administration of 800 microgram Cytotec half an hour after delivery.
Surgery: Evacuation of the uterus
Study Type
Interventional
Enrollment
200
Phase
- Phase 4
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 60 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Female
Description
Inclusion Criteria:
abortion at gestational age (ultrasound) 14+0 - 20+0
Exclusion Criteria:
Allergy to cytotec
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
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Side-effect
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Complication
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Secondary Outcome Measures
Outcome Measure |
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Quality of life
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Lars Alling Møller, MD phd, Rigshospitalet, Denmark
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Completion
January 1, 2009
Study Registration Dates
First Submitted
November 18, 2005
First Submitted That Met QC Criteria
November 18, 2005
First Posted (Estimate)
November 21, 2005
Study Record Updates
Last Update Posted (Estimate)
June 1, 2006
Last Update Submitted That Met QC Criteria
May 31, 2006
Last Verified
November 1, 2005
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- KF 01 279545
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.