Nerve block battle: which numbs better after gastric sleeve?
NCT ID NCT06798103
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested two types of nerve blocks—erector spinae plane block and thoracic paravertebral block—to see which one provides better pain relief after laparoscopic sleeve gastrectomy. Thirty adults having weight-loss surgery received one of the two blocks, and researchers measured how long it took before they needed extra pain medicine and how much pain they felt. The goal was to find the best way to control pain and help patients recover faster.
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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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30 people
The number who actually took part.
- Started
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Feb 2025
- Finished
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Jan 2026
- 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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21 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: 21 to 60 years. 2. Sex: males and females 3. Patients with American Society of Anesthesiologists physical status 4.classifications II-III undergoing laparoscopic sleeve gastrectomy under general anaesthesia. Exclusion Criteria: 1. Patient refusing to participate in the study. 2. Patients with bleeding disorders. 3. A history of relevant local anaesthetic allergy. 4. Patients with muscle diseases. 5. Evidence of local infection at site of injection. 6. Pre-existing chronic pain or cognitive dysfunction (which would impede accurate engagement with postoperative quality of recovery and analgesia assessment)
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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
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Ain shams University hospitals
Cairo, 02, Egypt
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