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Cornual Wedge Resection Outcome

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ClinicalTrials.gov Identifier: NCT03974841
Recruitment Status : Completed
First Posted : June 5, 2019
Last Update Posted : June 5, 2019
Sponsor:
Information provided by (Responsible Party):
Pınar Kadirogulları, Kanuni Sultan Suleyman Training and Research Hospital

Brief Summary:

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.


Condition or disease Intervention/treatment
Ectopic Pregnancy Laparoscopic Cornual Pregnancy Procedure: laparoscopic cornual resection

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Study Type : Observational
Actual Enrollment : 10 participants
Observational Model: Cohort
Time Perspective: Retrospective
Official Title: Cornual Wedge Resection for Interstitial Pregnancy and Postoperative Outcome
Actual Study Start Date : January 1, 2016
Actual Primary Completion Date : January 1, 2019
Actual Study Completion Date : January 1, 2019

Resource links provided by the National Library of Medicine



Intervention Details:
  • Procedure: laparoscopic cornual resection
    patients undergoing laparoscopic cornual resection due to cornual ectopic pregnancy


Primary Outcome Measures :
  1. Operation time [ Time Frame: surgery from start to end ]
    The duration of surgery of patients undergoing laparoscopic cornual resection due to cornual ectopic pregnancy

  2. amount of bleeding [ Time Frame: 48 hours ]
    The amount of hemorrhage in patients undergoing laparoscopic cornual resection due to cornual ectopic pregnancy



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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
postoperative results of patients who underwent laparoscopic cornual resection for cornual ectopic pregnancy, Patients forming the study group will be operated in the center for the last 3 years.
Criteria

Inclusion Criteria:

  • cornual ectopic pregnancy
  • Patients undergoing laparoscopic cornual wedge resection

Exclusion Criteria:

  • medical treatment area due to cornual pregnancy
  • laparotomy
  • conservatively managed patients

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): NCT03974841


Locations
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Turkey
Kanuni Sultan Süleyman Training and Research Hospital
Istanbul, Turkey, 33404
Sponsors and Collaborators
Kanuni Sultan Suleyman Training and Research Hospital

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Responsible Party: Pınar Kadirogulları, principal investigator, M.D, Department of Obstetrics and Gynecology, Kanuni Sultan Suleyman Training and Research Hospital
ClinicalTrials.gov Identifier: NCT03974841     History of Changes
Other Study ID Numbers: 2019.06
First Posted: June 5, 2019    Key Record Dates
Last Update Posted: June 5, 2019
Last Verified: June 2019

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No

Additional relevant MeSH terms:
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Pregnancy, Ectopic
Pregnancy, Cornual
Pregnancy Complications