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Which arm block works best for obese patients? new study aims to find out

NCT ID NCT07209995

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only This study
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study compares two ultrasound-guided nerve block techniques—retroclavicular infraclavicular block and axillary block—for pain control in 90 obese patients (BMI 30-40) having elbow or forearm surgery. Researchers will measure how long pain relief lasts, how much extra pain medicine is needed, and pain scores. The goal is to find which block provides better pain control for this specific group of patients.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
retroclavicular infraclavicular brachial plexus block or axillary block (local anesthetic injection)
What this could lead to
If this study shows one block is better, it could help doctors choose the best pain control method for obese patients having elbow surgery.
What could go wrong
This is a small, early-stage study with only 90 participants. The results may not apply to all patients or surgeries, and individual responses to the blocks can vary.

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

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

About 90 people

The number the study aims to enrol. It can still change while the study runs.

Started

Oct 2025

Expected to finish

Apr 2026

An estimate. End dates often move.

Lead sponsor

A government agency

The lead sponsor is a government body.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

21 to 45 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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Patients acceptance to share in the study. * Patients with ASA physical status I-II. * Obese patients (BMI 30-40 kg/m²) undergoing around and below elbow surgeries under regional anesthesia. * Patients requiring a single injection infraclavicular retroclavicular brachial plexus block or axillary block for around and below elbow surgeries. Exclusion Criteria: * Patients with a history of allergic reactions or contraindications to local anesthetics. * Patients with significant comorbidities (e.g., severe cardiovascular, neurological, or musculoskeletal disorders). * Patients with a history of previous shoulder or clavicle surgery that may distort anatomy and affect the efficacy of the block. * Pregnant or breastfeeding women. * Patients with a history of systemic infections or skin infections in the area of the block.

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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.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. 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.

    Open the record ↗

  3. 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

  • faculty of medicine,zagazig university Egypt

    Zagazig, 44519, Egypt