Cornual Wedge Resection Outcome

• Sponsor: Kanuni Sultan Suleyman Training and Research Hospital (Other)
• Overall Status: Completed
• CT.gov ID: NCT03974841
• Collaborator: (none)
• Enrollment: 10
• Location: 1
• Actual Duration (Months): 36
• Patients Per Site Per Month: 0.3

Study Details

Study Description

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	Phase
Ectopic Pregnancy; Laparoscopic; Cornual Pregnancy	Procedure: laparoscopic cornual resection

Study Design

• 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: Jan 1, 2016
• Actual Primary Completion Date: Jan 1, 2019
• Actual Study Completion Date: Jan 1, 2019

Outcome Measures

Primary Outcome Measures

1. Operation time [surgery from start to end]

   The duration of surgery of patients undergoing laparoscopic cornual resection due to cornual ectopic pregnancy

2. amount of bleeding [48 hours]

   The amount of hemorrhage in patients undergoing laparoscopic cornual resection due to cornual ectopic pregnancy

Eligibility Criteria

Criteria

• Ages Eligible for Study: 18 Years to 45 Years
• Sexes Eligible for Study: Female
• Accepts Healthy Volunteers: No

Inclusion Criteria:

• cornual ectopic pregnancy

• Patients undergoing laparoscopic cornual wedge resection

Exclusion Criteria:

• medical treatment area due to cornual pregnancy

• laparotomy

• conservatively managed patients

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Kanuni Sultan Süleyman Training and Research Hospital	Istanbul		Turkey	33404

Sponsors and Collaborators

• Kanuni Sultan Suleyman Training and Research Hospital

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: Pınar Kadirogulları, principal investigator, M.D, Department of Obstetrics and Gynecology, Kanuni Sultan Suleyman Training and Research Hospital
• ClinicalTrials.gov Identifier: NCT03974841
• Other Study ID Numbers: 2019.06
• First Posted: Jun 5, 2019
• Last Update Posted: Jun 5, 2019
• Last Verified: Jun 1, 2019

• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No
• Additional relevant MeSH terms: Pregnancy, Ectopic; Pregnancy, Cornual

Study Results

No Results Posted as of Jun 5, 2019