Nerve block or medicated packing: which eases sinus surgery pain better?
NCT ID NCT07555821
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests two ways to reduce pain after functional endoscopic sinus surgery. One method is a nerve block (sphenopalatine ganglion block) and the other is medicated nasal packing, both using the drugs bupivacaine and dexmedetomidine. Twenty adults scheduled for sinus surgery will be enrolled to see which approach provides better pain relief in the first 24 hours.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- bupivacaine and dexmedetomidine
- What this could lead to
- If it works, this could point toward a better way to manage pain after sinus surgery, reducing the need for strong painkillers.
- What could go wrong
- This is a small, early-phase trial with only 20 people, so results may not apply widely. Both methods are already used, so no major breakthrough is expected.
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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Phase 2/3
Runs two stages together: whether the treatment works, then large-scale confirmation.
- Participants
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About 20 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Apr 2026
An estimate. Start dates often move.
- Expected to finish
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Oct 2026
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.
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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 18 - 60 years 2. ASA physical status I -II 3. Patients scheduled for elective FESS Exclusion Criteria: 1. Allergy to drugs used 2. Coagulopathy or anticoagulant therapy 3. Severe cardiovascular, renal and hepatic disease 4. Chronic opioid use Pregnancy
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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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Assiut university hospital
Asyut, 161715, Egypt