CompletedNot Applicable

Personalized Prediction of Persistent Postsurgical Pain

United States2,500 participantsStarted 2021-09-10

Plain-language summary

P5 is planned as a prospective observational study, collecting evidence-based perioperative data on patient history and demographics, physical function, cognitive measures, psychological, and biological markers associated with increased pain susceptibility, and psychophysical measures of pain processing. The study will use daily ecologic momentary assessment (EMA) of physical and emotional parameters, and collect data on perioperative events. Follow up will occur 3 months and 6 months postoperatively.

Who can participate

Age range18 Years – 75 Years

SexALL

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Inclusion Criteria: * Adults age 18-75 who are candidates for major surgery (expected surgery duration \>1 hour, and expected overnight admission to the hospital), or having one of the following procedures, even if outpatient (total joint replacement, hysterectomy, inguinal hernia repair, breast surgery, or video-assisted thoracic surgery (VATS)). * Access to a smartphone Exclusion Criteria: * Participants who do not speak English

What they're measuring

Persistent Postsurgical Pain (PPSP)

Timeframe: up to 7 months following consent

Trial details

NCT IDNCT04864275

SponsorWashington University School of Medicine

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2025-09-30

View on ClinicalTrials.gov More Pain, Postoperative trials