← Back to Clinical Trials
Recruiting NCT06206148

NCT06206148 Comparison of Methods for Recording Post Operative Pain

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT06206148
Status Recruiting
Phase
Sponsor University of California, San Francisco
Condition Pain, Postoperative
Study Type INTERVENTIONAL
Enrollment 147 participants
Start Date 2024-03-01
Primary Completion 2026-06

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Given novel electronic pain recording deviceGiven Hand-written pain journalSmartphone app

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 147 participants in total. It began in 2024-03-01 with a primary completion date of 2026-06.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief 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.

Eligibility Criteria

Inclusion Criteria: * Patient over 18 years old Exclusion Criteria: * Patient cannot use a smartphone * Patient cannot use his hands to write or press a button * Patient has a nerve catheter (has no pain) * Altered mental status * Neuropathy causing loss of pain sensation

Contact & Investigator

Central Contact

Meir T Marmor, MD

✉ meir.marmor@ucsf.edu

📞 6504776238

Principal Investigator

Meir T Marmor, MD

PRINCIPAL INVESTIGATOR

University of California, San Francisco

Frequently Asked Questions

Who can join the NCT06206148 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Pain, Postoperative. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06206148 currently recruiting?

Yes, NCT06206148 is actively recruiting participants. Contact the research team at meir.marmor@ucsf.edu for enrollment information.

Where is the NCT06206148 trial being conducted?

This trial is being conducted at San Francisco, United States.

Who is sponsoring the NCT06206148 clinical trial?

NCT06206148 is sponsored by University of California, San Francisco. The principal investigator is Meir T Marmor, MD at University of California, San Francisco. The trial plans to enroll 147 participants.

Related Trials

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology