New drug combo may ease liposuction pain without opioids
NCT ID NCT04862845
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This completed phase 1 trial tested whether combining duloxetine and pregabalin can reduce pain after liposuction surgery. 90 adults were given either the drug combo, pregabalin alone, or a placebo before and after surgery. The goal was to see if the combo lowers the need for morphine and improves recovery. Results could point to a safer, opioid-free pain management option.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- duloxetine and pregabalin
- What this could lead to
- If it works, this could offer a safer, non-opioid way to manage pain after liposuction surgery.
- What could go wrong
- This is a small, early-phase trial (phase 1) with only 90 participants. The results may not apply to other surgeries or larger populations, and side effects from the drug combination are possible.
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
-
90 people
The number who actually took part.
- Started
-
Jul 2021
- Finished
-
Jan 2026
- 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
-
18 to 50 years
- Sex
-
Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
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: * Patients aged from 18 to40 years. * ASA I-II. * undergoing elective mega -liposuction surgery * BMI from 18 to 50 kg/m2 2\. Exclusion criteria: * Patient refusal * Contraindication or chronic use (consistent use for longer than 3 months) to any of the study drugs ASA III-IV. * Patients aged less than 18 or more than 50. * Body mass index \>50. * Suffered from severe psychiatric disease or drug addiction; * Chronic opioid consumption, * a history of regular sedatives or anticonvulsants intake, serious organ disease or dysfunction * inability to use a PCA device * History of parenteral or oral analgesic intake within the last 48hours.
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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.
Contacts and locations
Locations
-
facility of medicine Cairo university
Cairo, 12613, Egypt
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