Fake pills, real relief? placebo study aims to cut opioid use after hip surgery
NCT ID NCT07373210
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether taking placebo pills alongside standard opioid painkillers can reduce pain and opioid use in adolescents and young adults after hip surgery. 64 participants will either receive the placebo plus usual care or usual care alone. The goal is to see if the placebo effect can help manage pain and lower the need for opioids.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- open-label placebo pills
- What this could lead to
- If it works, this could offer a way to reduce opioid use after surgery by harnessing the placebo effect, even when patients know the pills are fake.
- What could go wrong
- This is a small, early-stage trial with only 64 participants, so results may not apply widely. The placebo effect is unpredictable and may not significantly reduce pain or opioid consumption.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 64 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Dec 2026
An estimate. Start dates often move.
- Expected to finish
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Mar 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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13 to 40 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Aged 13 to 40 years old, and * Undergo primary Bernese Periacetabular osteotomy (PAO) for symptomatic developmental dysplasia of the hip (DDH), and * Opioid-naïve prior to operation, and * Capable of completing study procedures, including daily pain and medication diaries as well as weekly questionnaires. Exclusion Criteria: * Undergoing PAO revision or any concurrent major surgical procedure * History of opioid use, substance use disorders, or alcohol abuse * Those with cognitive or physical impairments that would interfere with providing their own consent and the completion of study-related tasks * Pregnant individuals or those planning to become pregnant during the study period
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Get notified about this study
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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University of California San Francisco
RECRUITINGSan Francisco, California, 94158, United States
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