New tool aims to curb opioid overprescribing after surgery
NCT ID NCT07510373
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests a tool called DOTS that helps doctors create a personalized plan to reduce opioid painkillers after orthopedic surgery. The tool is built into the hospital's computer system and includes a taper schedule, a patient handout, and phone support after discharge. Researchers will compare patients whose doctors used DOTS to those who received usual care, looking at how many opioids are prescribed and how well patients manage pain and recovery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Discharge Opioid Taper Support (DOTS) tool
- What this could lead to
- If successful, this could provide a simple, scalable way to reduce unnecessary opioid prescriptions after surgery, lowering the risk of long-term opioid use.
- What could go wrong
- This is a small, early-stage trial with only 42 providers, so results may not apply broadly. The intervention relies on doctors following recommendations, which may not always happen.
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 42 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Apr 2026
- Expected to finish
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Apr 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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18 years and older
- 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 (Aim 1): * Age ≥ 18 years * Any orthopedic surgery during hospitalization * No pre-operative opioid use (no opioids in EHR in past 1 month) Exclusion Criteria (Aim 1): * Opioid Use Disorder \[by International Classification of Diseases, 10th revision (ICD-10), in past 6 months} * Cancer (by ICD-10, in past 6 months) * Receiving hospice care (by ICD-10, in past 6 months) Inclusion Criteria (Aim 2): * Meets criteria for inclusion in Aim 1 Exclusion Criteria (Aim 2): * Not fluent in English * Do not manage their own medications * Unable to provide consent over the phone * Orthopedic surgery due to cancer-related bone disease * No pre-operative opioid use (no opioids per New York state prescription drug monitoring program in past 1 month)
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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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Montefiore Wakefield Campus
RECRUITINGThe Bronx, New York, 10466, United States
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