Cornual Wedge Resection Outcome

Ectopic Pregnancy Clinical Trial

Official title:

Cornual Wedge Resection for Interstitial Pregnancy and Postoperative Outcome

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03974841
• Other study ID #: 2019.06
• Status: Completed
• Start date: January 1, 2016
• Est. completion date: January 1, 2019

Study information

• Verified date: June 2019
• Source: Kanuni Sultan Suleyman Training and Research Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial 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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 10
• Est. completion date: January 1, 2019
• Est. primary completion date: January 1, 2019
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years to 45 Years

Eligibility

Inclusion Criteria:

• cornual ectopic pregnancy

• Patients undergoing laparoscopic cornual wedge resection

Exclusion Criteria:

• medical treatment area due to cornual pregnancy

• laparotomy

• conservatively managed patients

Related Conditions & MeSH terms

• Cornual Pregnancy
• Ectopic Pregnancy
• Laparoscopic
• Pregnancy, Ectopic

Intervention

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

Locations

Country	Name	City	State
Turkey	Kanuni Sultan Süleyman Training and Research Hospital	Istanbul

Sponsors (1)

Lead Sponsor	Collaborator
Kanuni Sultan Suleyman Training and Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Operation time	The duration of surgery of patients undergoing laparoscopic cornual resection due to cornual ectopic pregnancy	surgery from start to end
Primary	amount of bleeding	The amount of hemorrhage in patients undergoing laparoscopic cornual resection due to cornual ectopic pregnancy	48 hours