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Which arm block spares the diaphragm? new study pits two techniques Head-to-Head
NCT ID NCT07386470
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study compared two ultrasound-guided nerve block techniques for hand, wrist, or forearm surgery to see which one causes less temporary diaphragm paralysis. 91 adults were randomly assigned to receive either a costoclavicular or lateral sagittal infraclavicular block. The goal is to help anesthesiologists choose the safer option for patients.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Ultrasound-guided infraclavicular nerve block (procedure)
- What this could lead to
- If one technique causes less diaphragm weakness, it could help anesthesiologists choose a safer nerve block for arm surgeries.
- What could go wrong
- This is a small, completed study with 91 participants. Results may not apply to all patients or surgeries, and individual responses to nerve blocks 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
-
91 people
The number who actually took part.
- Started
-
Oct 2022
- Finished
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Apr 2023
- 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 80 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.
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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: * Adults aged 18-80 years * ASA physical status I-III * Scheduled for forearm, wrist, or hand surgery * Planned infraclavicular brachial plexus block Exclusion Criteria: * Refusal of regional anesthesia * Known allergy to local anesthetics * Infection at the block site * Pre-existing neurological deficit in the operative limb * Severe pulmonary disease * Coagulopathy or sepsis * BMI \> 40 kg/m² * Psychiatric disorders
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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
-
Gazi University Faculty of Medicine, Department of Anesthesiology and Reanimation
Ankara, Ankara, 06560, Turkey (Türkiye)
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Ultrasound reveals how a neck nerve block may impact the diaphragm
- Pulse wave test may replace needles to check nerve block success
- New study aims to find safer pain block for shoulder surgery
- Shoulder block study checks for breathing side effects
- Arm angle may make or break your nerve block