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Early Pregnancy Failure: Factors Affecting Successful Medical Termination Treatment

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00782860
First Posted: October 31, 2008
Last Update Posted: March 31, 2009
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Western Galilee Hospital-Nahariya
  Purpose
The main purpose of our study was to which determine factors, those measured by ultrasound and also demographic and clinical factors (age, number of previous pregnancies, abortions and deliveries) predict outcome of medical treatment for early pregnancy failure. Our hypothesis was that gestational sac volume predicts outcome of medical treatment for early pregnancy failure.

Condition
Early Pregnancy Failure

Study Type: Observational
Study Design: Time Perspective: Prospective

Further study details as provided by Western Galilee Hospital-Nahariya:

Primary Outcome Measures:
  • An empty uterus or an endometrial lining with thickness of less than 30mm.

Groups/Cohorts
unsuccessful termination
unsuccessful termination of early pregnancy failure with Misoprostol
successful termination
successful termination of early pregnancy failure with Misoprostol

  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 45 Years   (Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Women with missed abortion or anembryonic pregnancy, with existing intrauterine pregnancy sac
Criteria

Inclusion Criteria:

  • Crown rump length (CRL) is appropriate to less than 12 weeks.
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00782860


Locations
Israel
Western Galilee Hospital-Nahariya
Nahariya, Israel, 22100
Sponsors and Collaborators
Western Galilee Hospital-Nahariya
  More Information

ClinicalTrials.gov Identifier: NCT00782860     History of Changes
Other Study ID Numbers: 03-08-2008
First Submitted: October 28, 2008
First Posted: October 31, 2008
Last Update Posted: March 31, 2009
Last Verified: March 2009

Keywords provided by Western Galilee Hospital-Nahariya:
Early pregnancy failure
Misoprostol
Gestational sac volume

Additional relevant MeSH terms:
Misoprostol
Abortifacient Agents, Nonsteroidal
Abortifacient Agents
Reproductive Control Agents
Physiological Effects of Drugs
Anti-Ulcer Agents
Gastrointestinal Agents
Oxytocics