Opioid study aims to personalize pain treatment for back pain sufferers
NCT ID NCT02824276
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study looked at how oral opioids like oxycodone or morphine affect pain sensitivity in 35 adults with chronic low back pain. Participants received either the opioid or a placebo to measure changes in pain perception. The goal is to understand individual differences and improve how doctors prescribe painkillers.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Oxycodone or morphine sulfate immediate release (MSIR)
- What this could lead to
- If successful, this could help doctors tailor opioid prescriptions to individual patients for better pain relief.
- What could go wrong
- This is a small, early-phase study with only 35 participants, so results may not apply to everyone. Opioids also carry risks like addiction and side effects.
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
-
Phase 1
The first testing in people. Mainly checks safety and dose, usually in a small group.
- Participants
-
35 people
The number who actually took part.
- Started
-
Jan 2017
- Finished
-
Dec 2025
- Lead sponsor
-
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
-
25 to 65 years
- Sex
-
Anyone
- Healthy volunteers
-
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: 1. age 25-65 2. CLBP lasting for more than 6 months as the primary complaint 3. typical pain ratings ≥ 4/10 on a visual analogue scale 4. candidate for oral opioid therapy as assessed at the BWH Pain Management Center 5. able to speak and understand English. Exclusion Criteria: 1. evidence of delirium, dementia, psychosis, or other cognitive impairment preventing completion of study procedures 2. current (i.e., active) substance use disorder (SUD) 3. past history of persistent opioid use (i.e., opioid use for more than 6 months) given that this could affect the biological systems of interest in the present study 4. history of myocardial infarction or other serious cardiovascular condition 5. current peripheral neuropathy 6. current pregnancy, or intention to become pregnant during the study 7. current intrathecal pump.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Low back pain are added.
Genom att skicka in godkänner du våra Användarvillkor
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.
Contacts and locations
Locations
-
Brigham and Women's Hospital
Boston, Massachusetts, 02467, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Radiofrequency device tested as Add-On for stubborn back pain
- Back muscles hold clues for treating recurrent low back pain
- Skip the GP? physiotherapy first for back pain put to the test
- Can yoga ease back pain when recovery looks unlikely?
- Can a second injection target the source of stubborn back pain?
- Can releasing a deep back muscle ease pain and help you breathe better?