Central Sensitization and Outcome of Endometriosis Surgery

Completed

• Conditions: Endometriosis

• Registration Number: NCT04144998
• Lead Sponsor: Benno Rehberg-Klug

Brief Summary

This study will evaluate whether the degree of central sensitization as measured by the questionnaire "central sensitization inventory CSI" is related to the outcome of surgical endometriosis treatment

Detailed Description

Not available

Study Timeline

• Study Start: 2019-10-01
• Study First Submitted: 2019-10-28
• Study First Submitted QC: 2019-10-28
• Study First Posted: 2019-10-30
• Primary Completion: 2021-12-31
• Study Completion: 2022-06-13
• Status Verified: 2022-07
• Last Update Submitted: 2022-07-20
• Last Update Posted: 2022-07-21

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 71

Inclusion Criteria

• Primary surgery because of pelvic/abdominal pain under suspected diagnosis of and with the aim to confirm endometriosis
• Elective abdominal surgery in women with pelvic/abdominal pain and confirmed endometriosis

Exclusion Criteria

• Patient is unable to give consent
• Cognitive impairment
• Patient outcomes questionnaire is not available in a language that the patient knows.
• Secondary surgery due to complications
• Endometriosis Surgery due to infertility

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
endometriosis health profile EHP-30 pain subscale	6 months	Pain subscale of the questionnaire "endometriosis health profile" EHP-30, scale from 0-100, higher values indicate worse health status

Secondary Outcome Measures

Name	Time	Method
other subscales of the endometriosis health profile EHP-30	6 months	control and powerlessness scale, emotional well-being scale, social support scale, self-image scale, all scales from 0-100, higher values indicate worse health status

Trial Locations

Locations (1)

Hôpitaux Universitaires de Genève; 🇨🇭 Geneva, Switzerland