- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01270334
Effect of Vaginal PH on Treatment Effectiveness With Misoprostol for First Trimester Missed Abortions
January 4, 2011 updated by: HaEmek Medical Center, Israel
vaginal PH has an effect on the effectiveness of treatment with misoprostol given vaginally for missed abortions in the first trimester
Study Overview
Study Type
Observational
Enrollment (Anticipated)
400
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: shira baram, dr
- Phone Number: 972-4-6494035
- Email: shira_ba@clalit.org.il
Study Locations
-
-
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Afula, Israel
- Haemel Medical Center
-
Contact:
- shira baram, md
- Phone Number: 972-4-6494035
-
Principal Investigator:
- shira baram, md
-
-
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 50 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Female
Sampling Method
Non-Probability Sample
Study Population
women dignosed with missed abortion in the first trimester
Description
Inclusion
- missed abortion under 8 weeks by sac diameter over 18 years old informed concent given
Exclusion Criteria:
- missed abortion over 8 weeks hypersensitivity for PG vaginal bleeding suspected EUP IUD heart disease, HTN, cerebral vascular disease, epilepsy intrauterine infection clooting disorder under 18
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
- Observational Models: Case-Control
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
ph above cutoff
|
meassuring ph USING PROBE
|
PH under cutoff
|
meassuring ph USING PROBE
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
treatment failure- need for D&C
Time Frame: 2 weeks
|
2 weeks
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
side effects, need foe analgetics, time for compliting abortion
Time Frame: 2 weeks
|
2 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 Start
February 1, 2011
Study Registration Dates
First Submitted
January 4, 2011
First Submitted That Met QC Criteria
January 4, 2011
First Posted (Estimate)
January 5, 2011
Study Record Updates
Last Update Posted (Estimate)
January 5, 2011
Last Update Submitted That Met QC Criteria
January 4, 2011
Last Verified
January 1, 2011
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- cytoph
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.
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