Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

Cure My Disease

Don't miss your cure!

 Log in / Sign up

New nerve block combo may offer safer pain relief for broken collarbone surgery

NCT ID NCT07548775

Symptom relief Sponsor: Udayana University Source: ClinicalTrials.gov ↗

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
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jun 27, 2026

Summary

This study compares two types of nerve blocks for pain relief during collarbone surgery. The standard block can sometimes cause breathing problems. Researchers are testing a new combination that targets the collarbone area directly, hoping it will provide the same pain relief with fewer side effects. The trial involves 34 adults undergoing surgery for a broken collarbone.

What this could mean

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

Active substance
nerve block (superficial cervical block + clavipectoral block)
What this could lead to
If successful, this could offer a safer, equally effective pain relief option for clavicle surgery, reducing the risk of breathing problems.
What could go wrong
This is a small, early-phase study with only 34 participants, so results may not apply to everyone. The new block might not provide as long-lasting pain relief as the standard technique.

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

34 people

The number who actually took part.

Started

Apr 2026

Expected to finish

Jul 2026

An estimate. End dates often move.

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

20 to 60 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: * Surgical Requirement: Patients scheduled to undergo elective or emergency surgery for clavicle fracture fixation (Open Reduction Internal Fixation). * Physical Status: Patients classified as American Society of Anesthesiologists (ASA) Physical Status I or II (healthy patients or those with mild systemic disease). * Age Range: Adult patients aged between 20 and 60 years. * Body Mass Index (BMI): Patients with a BMI within the range of 18.5 to 30kg/m2. * Cognitive Status: Patients who are conscious, cooperative, and able to communicate effectively to provide informed consent and report pain scores (VAS). * Consent: Patients who have voluntarily signed the written informed consent form after a full explanation of the procedure. Exclusion Criteria: * Hypersensitivity or known allergy to local anesthetics. Patients presenting with respiratory compromise or significant pulmonary dysfunction. * Clinical history of coagulopathy or blood coagulation disorders. * Active infection at the site of needle insertion/puncture. * Chronic opioid consumption, defined as continuous use for three consecutive months. * Refusal to provide informed consent or participate in the study.

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for Clavicle fracture are added.

Vår säkerhetsrekommendation!

Genom att skicka in godkänner du våra Användarvillkor

Conditions

The condition(s) this trial relates to.

Pain, Postoperative

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Clavicle fracture Postoperative pain Regional anesthesia block

Contacts and locations

Locations

  • Ngoerah Hospital

    Denpasar, Bali, 80114, Indonesia

More trials for these conditions

Other studies related to the condition(s) this trial covers.