Investigation of excisional surgery versus ablation for the treatment of chronic pelvic pain in endometriosis

Not Applicable

Recruiting

• Conditions: Endometriosis.; Endometriosis

• Registration Number: IRCT20200518047489N1
• Lead Sponsor: Esfahan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 15 June 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 60

Inclusion Criteria

Age above 18 years and less than 40 years
Lacking hormone therapy within the previous three months
Willingness for participation in the study
Chronic pelvic pain for more than 6 months
Normal abdominopelvic, uterine and ovarian ultrasonographic imaging
No medical history of diabetes or hypertension

Exclusion Criteria

Lacking gross endometriosis evidence in laparoscopy
Endometriosis grades III and IV in laparoscopy

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain score due to dysmenorrhea. Timepoint: At baseline, within 6 months and within 12 months. Method of measurement: Visual analogue scale questionnaire.;Dysparonia. Timepoint: At baseline, within 6 months and within 12 months. Method of measurement: Visual analogue scale questionnaire.;Dyschezia. Timepoint: At baseline, within 6 months and within 12 months. Method of measurement: Visual analogue scale questionnaire.;Pain in non-menstrual time. Timepoint: At baseline, within 6 months and within 12 months. Method of measurement: Visual analogue scale questionnaire.