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NCT06206148

Comparison of Methods for Recording Post Operative Pain

Comparison of Methods for Recording Post Operative Pain: A Prospective Randomized Trial
University of California, San Francisco·ClinicalTrials.gov·device·Device trialNot yet recruiting
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Study focus
Disease/Condition
Pain, Postoperative
Drug/Device/Intervention
Given novel electronic pain recording device
Study type
Interventional
Intervention type
device
Sponsor & location
Primary sponsor
University of California, San Francisco
Location
San Francisco, United States of America
Timeline & enrollment
Phase
N/A
Start date
Mar 01, 2024
End date
Jun 01, 2024
Enrollment
147 participants
Primary outcome

Comparing Methods for Pain Score collection

Summary

The purpose of the current study is to identify the optimal method of collection of pain
 intensity data. The study will compare three collection methods: a hand-written pain journal,
 a smartphone app, and a novel electronic pain recorder device. Patients will be randomly
 assigned to one of three methods and instructed to record their pain level as often as they
 like. The number of pain intensity recordings per day will then be compared across groups.

ICD-10 classifications
During surgical operationDuring surgical operationDuring surgical operationPain, unspecifiedPostoperative intestinal obstruction
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT06206148
Type
Device Trial
About this record

Access comprehensive clinical trial information for NCT06206148 through Pure Global AI's free database. This phase not specified trial is sponsored by University of California, San Francisco and is currently Not yet recruiting. The study focuses on Pain, Postoperative. Target enrollment is 147 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.