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Nerve block may cut opioid use after neck surgery

NCT ID NCT07694180

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

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jul 09, 2026 · Last updated Jul 10, 2026 · Updated 1 time

Summary

This study looks at whether a specific nerve block, called the Serratus Posterior Superior Intercostal Plane Block, can reduce pain and the need for strong painkillers after anterior cervical discectomy and fusion (ACDF) surgery. Researchers will compare outcomes between patients who receive the block and those who do not. The goal is to find a safer, more effective way to manage post-surgery pain.

What this could mean

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

Active substance
Serratus Posterior Superior Intercostal Plane Block (SPSIP block)
What this could lead to
If effective, this nerve block could offer better pain control and reduce reliance on opioids after cervical disc surgery.
What could go wrong
This is a small observational study, so results may not apply broadly. The block may not significantly improve pain or reduce opioid use.

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 66 people

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

Expected to start

Jun 2026

An estimate. Start dates often move.

Expected to finish

Jan 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.

Who is studied

The study population will consist of adult patients aged 18-70 years with ASA physical status I-III who are scheduled to undergo elective anterior cervical discectomy and fusion (ACDF) surgery under general anesthesia at Samsun City Hospital. Eligible patients who provide written informed consent and meet the study inclusion criteria will be enrolled consecutively during the study period

Ages

18 to 70 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 aged between 18 and 70 years. * American Society of Anesthesiologists (ASA) physical status I, II, or III. * Patients scheduled for elective anterior cervical discectomy and fusion (ACDF) surgery under general anesthesia. * Patients who provide written informed consent and agree to participate in the study. Exclusion Criteria: * Patients with a history of bleeding diathesis or those receiving anticoagulant therapy. * Patients with a known allergy or hypersensitivity to local anesthetics or opioid medications. * Patients with infection at the planned block site. * Patients with a history of previous cervical spine surgery. * Patients with a history of gabapentinoid or corticosteroid use within the last 3 weeks.

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Conditions

The condition(s) this trial relates to.

Acute Pain

As listed by the trial registrant

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

Acute pain Servical disc herniation

How to take part

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  1. The official record

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