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Central Sensitization and Outcome of Endometriosis Surgery

B

Benno Rehberg-Klug

Status

Completed

Conditions

Endometriosis

Treatments

Diagnostic Test: central sensitization inventory (questionnaire)

Study type

Observational

Funder types

Other

Identifiers

NCT04144998
EndoPROMPT

Details and patient eligibility

About

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

Enrollment

71 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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