Actively Recruiting

Phase Not Applicable
Age: 13Years - 40Years
All Genders
NCT07373210

Open-label Placebo for Pain Management in Adolescents and Young Adults Undergoing Bernese Periacetabular Osteotomy

Led by University of California, San Francisco · Updated on 2026-04-29

64

Participants Needed

1

Research Sites

69 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

In this randomized controlled trial, 64 participants undergoing PAO at UCSF will be enrolled and randomized to receive either COLP plus treatment as usual (TAU) or TAU alone. Patients in the COLP arm will receive placebo pills alongside prescribed opioids and at scheduled intervals, beginning on postoperative day one. Weekly follow-up will be conducted for six weeks postoperatively via remote surveys and video visits.

CONDITIONS

Official Title

Open-label Placebo for Pain Management in Adolescents and Young Adults Undergoing Bernese Periacetabular Osteotomy

Who Can Participate

Age: 13Years - 40Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged 13 to 40 years old
  • Undergo primary Bernese Periacetabular osteotomy (PAO) for symptomatic developmental dysplasia of the hip (DDH)
  • Opioid-nafve prior to operation
  • Capable of completing study procedures, including daily pain and medication diaries and weekly questionnaires
Not Eligible

You will not qualify if you...

  • Undergoing PAO revision or any concurrent major surgical procedure
  • History of opioid use, substance use disorders, or alcohol abuse
  • Cognitive or physical impairments interfering with consent or study tasks
  • Pregnant individuals or those planning pregnancy during the study period

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of California San Francisco

San Francisco, California, United States, 94158

Actively Recruiting

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Research Team

T

Tripta Rughwani

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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