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New nerve block technique could ease neck surgery pain

NCT ID NCT07539935

Symptom relief Sponsor: Sohag 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 24, 2026 · Last updated Jun 27, 2026 · Updated 2 times

Summary

This study tests whether an ultrasound-guided nerve block using bupivacaine can reduce pain after neck surgery better than standard painkillers. Sixty adults aged 18 to 60 undergoing elective neck surgery will be randomly assigned to receive either the nerve block or a placebo injection plus paracetamol. Pain levels and opioid use will be tracked for 24 hours after surgery.

What this could mean

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

Active substance
bupivacaine
What this could lead to
If it works, this could offer a more effective way to manage pain after neck surgery, reducing the need for opioids.
What could go wrong
This is a small, single-center trial with only 60 participants. The results may not apply to all neck surgeries or patients, and nerve blocks carry rare risks like infection or allergic reaction.

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

Phase 4

Runs after approval, following long-term safety and how well the treatment works in everyday use.

Participants

About 60 people

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

Started

Mar 2026

Expected to finish

Oct 2027

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

18 to 60 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

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: * The study include all patients between 18 and 60 years of age who underwent elective neck surgery under general anesthesia Exclusion Criteria: * 1\. Patient refusal . 2. Patient with significant neurological , psychological disease . 3. patient known allergy to local anesthesia . 4. Patient uncorrected coagulapathy or anticoagulant therapy . 5. Patient with sever neck deformity . 6. Patient with infection at site of injection . 7. Patient with sever respiratory disease . 8. patients with regular use of analgesic medications

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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.

Postoperative pain

Contacts and locations

Locations

  • Faculty of medicine, Sohag University.

    Sohag, Egypt

More trials for these conditions

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