- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03974841
Cornual Wedge Resection Outcome
Cornual Wedge Resection for Interstitial Pregnancy and Postoperative Outcome
Cornual pregnancy is a rare form of ectopic pregnancy that accounts for 2% to 4% of ectopic pregnancies, with a mortality rate between 2.0% and 2.5%. Traditionally, interstitial pregnancies were treated by laparotomy with cornial resection or hysterectomy. However, nowadays, increasingly interstitial pregnancies are treated by laparoscopic cranial resection.
Although this technique can potentially protect the fertility of the patient, it carries a serious risk of bleeding and requires a surgical experience.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
-
Istanbul, Turkey, 33404
- Kanuni Sultan Suleyman Training and Research Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- cornual ectopic pregnancy
- Patients undergoing laparoscopic cornual wedge resection
Exclusion Criteria:
- medical treatment area due to cornual pregnancy
- laparotomy
- conservatively managed patients
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Retrospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Operation time
Time Frame: surgery from start to end
|
The duration of surgery of patients undergoing laparoscopic cornual resection due to cornual ectopic pregnancy
|
surgery from start to end
|
amount of bleeding
Time Frame: 48 hours
|
The amount of hemorrhage in patients undergoing laparoscopic cornual resection due to cornual ectopic pregnancy
|
48 hours
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2019.06
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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