New painkiller combo could make knee surgery recovery easier
NCT ID NCT07131579
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests whether adding dexmedetomidine to spinal anesthesia can extend pain relief after knee surgery. One hundred adults scheduled for elective knee surgery will receive either the drug or a placebo. Researchers will measure how long it takes before patients need additional pain medication.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Dexmedetomidine
- What this could lead to
- If it works, this could offer a way to reduce pain after knee surgery without strong side effects like breathing problems.
- What could go wrong
- This is a small, early-stage study. The drug may not provide meaningful extra pain relief, and it could cause sedation or low blood pressure.
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 100 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jan 2026
- Expected to finish
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Aug 2027
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 to 60 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: * Age 18-60 years * American Society of Anesthesiologists (ASA) Physical Status Classification System I or II * Scheduled for elective knee surgery under spinal anesthesia * Body mass index (BMI) 18-30 kg/m² * Able to provide informed consent Exclusion Criteria: * Pregnant or lactating women * Hypersensitivity to dexmedetomidine * Chronic kidney diseases serum creatinine \>1.5 mg\\dl or Patient has known renal disease * Chronic opioid or sedative use * Any cardiac conduction abnormalities * Uncontrolled arterial hypertension * Neuropathy * Diabetes mellitus * Impaired perfusion of the operative limb (Edema, Peripheral vascular Disease e.g "Raynaud Phenomenon") * History or recent lower limb deep venous thrombosis (DVT) or Phlebitis * Infection or vascular access limitation in the operated lower limbs * Any contraindication of spinal anesthesia e.g "Coagulopathy" * Any contraindications for tourniquet e.g "sickle cell anemia"
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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
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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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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Faculty of Medicine-Mansoura University
Al Mansurah, Egypt
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