At a glance
ClinicalIndex Comparison RecordN/ACompleted· 2,500 enrolled
Drug / intervention
Not specified
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Personalized Prediction of Persistent Postsurgical Pain
In Brief
An observational study for Pain, Postoperative. Completed, enrolled 2,500 participants across 1 site.
Detailed 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.
Study Details
Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsPain, Postoperative
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
20222023202420252026
First PostedApr 2021
Enrollment StartSep 2021
Primary CompletionSep 2025
TodayJul 2026
First PostedApr 28, 2021
Enrollment StartSep 10, 2021
Primary CompletionSep 30, 2025
TodayJul 2, 2026
Enrollment to primary: 4.1 yearsPosted 5.2 years ago