Central Sensitization and Outcome of Endometriosis Surgery

NCT ID: NCT04144998

Last Updated: 2022-07-21

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 71 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2019-10-01
• Study Completion Date: 2022-06-13

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

Conditions

Endometriosis

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Interventions

central sensitization inventory (questionnaire)

T.G. Mayer, R. Neblett, H. Cohen, et al. The development and psychometric validation of the central sensitization inventory Pain Pract, 12 (2012), pp. 276-285

Intervention Type: DIAGNOSTIC_TEST

Eligibility Criteria

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

• Minimum Eligible Age: 18 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

Benno Rehberg-Klug

OTHER

Sponsor Role: lead

Responsible Party

Benno Rehberg-Klug

Dr. Benno Rehberg-Klug, Principal Investigator

Responsibility Role: SPONSOR_INVESTIGATOR

Locations

Hôpitaux Universitaires de Genève

Geneva, , Switzerland

Countries

Switzerland

Other Identifiers

EndoPROMPT

Identifier Type: -

Identifier Source: org_study_id