ClinicalTrials.Veeva

Menu

Study to Test the Value of a Pain Modulation Test in Predicting Persistent Postoperative Pain After Breast Cancer Surgery (PREDO)

University Hospitals (UH) logo

University Hospitals (UH)

Status

Completed

Conditions

Chronic Pain
Acute Pain

Treatments

Other: comprehensive preoperative testing for risk factors of persistent postoperative pain

Study type

Observational

Funder types

Other

Identifiers

NCT01767168
CER 10-218
matped 10-054 (Other Identifier)

Details and patient eligibility

About

The purpose of this study is to test the hypothesis that a preoperative test of pain modulation predicts persistent pain 4 months after breast cancer surgery. In addition, a risk score for the prediction of persistent pain will be developed from parameters available before surgery.

Enrollment

200 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • age >=18 years
  • American Society of Anesthesiology functional status I-III
  • able to read and understand the information sheet and give informed consent

Exclusion criteria

none

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems