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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00782860
Other study ID # 03-08-2008
Secondary ID
Status Completed
Phase N/A
First received October 28, 2008
Last updated March 30, 2009

Study information

Verified date March 2009
Source Western Galilee Hospital-Nahariya
Contact n/a
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Observational

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Completed
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria:

- Crown rump length (CRL) is appropriate to less than 12 weeks.

Study Design

Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Israel Western Galilee Hospital-Nahariya Nahariya

Sponsors (1)

Lead Sponsor Collaborator
Western Galilee Hospital-Nahariya

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary An empty uterus or an endometrial lining with thickness of less than 30mm. No
See also
  Status Clinical Trial Phase
Terminated NCT03212352 - Comparing Two Medical Treatments for Early Pregnancy Failure. Phase 4
Completed NCT03178682 - Ultrasound Predictors of Early Pregnancy Failure in Patients With Recurrent Pregnancy Loss N/A
Terminated NCT00468299 - MiMi: A Randomized Trial of Mifepristone and Misoprostol for Treatment of Early Pregnancy Failure N/A