Shoulder surgery nerve block showdown: which one spares your diaphragm?
NCT ID NCT07553611
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study compares four types of nerve blocks used during arthroscopic shoulder surgery to see which one causes the least temporary diaphragm paralysis and leads to better recovery. Researchers will measure breathing function, pain levels, opioid use, and overall recovery quality in 88 adults aged 18-65. The goal is to identify the safest and most effective block for routine use.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this study could help doctors choose the best nerve block for shoulder surgery, reducing breathing problems and improving recovery.
- What could go wrong
- This is a small observational study, not a treatment trial. Results may not apply to all patients, and the findings are not a guarantee of better outcomes.
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.
- Participants
-
About 88 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Apr 2026
- Expected to finish
-
Nov 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.
Who is studied
It is planned to include ASA score I-III, aged 18-65 years, who are planned to undergo elective arthroscopic surgery
- Ages
-
18 to 65 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 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: * aged 18-65 years * American Society of Anaesthesiology (ASA) score I-III * body mass index (BMI) \<30kg/m2 * scheduled for elective arthroscopic surgery Exclusion Criteria: * ASA score ≥4 * BMI ≥30 kg/m2 * declining to give written informed consent * controendications for block application * history of mental or neurological disease, severe liver and/or kidney disease * history of moderate or severe pulmonary disease * abnormal preoperative chest X-ray findings * scheduled for emergency surgery
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Arthroscopic shoulder surgery are added.
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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
-
The places running it
1 site. The list below names each one and where it is.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
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
-
University of Health Sciences, Antalya Training and Research Hospital
RECRUITINGAntalya, Muratpaşa, Turkey (Türkiye)
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Which nerve block cuts opioid use in kids after surgery?
- Can a steroid extend pain relief after shoulder surgery?
- Spinal block showdown: can one injection method beat another for Post-Surgery pain?
- Could a simple mineral cut opioid use in Kids' surgery?
- One injection or many? a test to ease breast surgery pain
- Can a new nerve block beat standard pain relief for shoulder surgery?