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Extra nerve block may cut opioid use after hip surgery

NCT ID NCT06839742

Symptom relief Sponsor: Samsun 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
Running, but no longer taking on new participants.
Completed This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 looked at whether adding a deep gluteal nerve block to a standard hip block can improve pain relief and reduce the need for strong painkillers after hip fracture surgery. 68 adults having hip surgery under spinal anesthesia took part. Researchers measured pain scores and how much morphine patients used in the first 24 hours after surgery.

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

68 people

The number who actually took part.

Started

Feb 2025

Finished

Dec 2025

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 90 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: * Volunteering to participate in the study * Patients between the ages of 18-90 * ASA I, II, III * Patients whose surgery duration does not exceed 2 hours * Patients who will undergo surgery under spinal anesthesia Exclusion Criteria: * Patients who do not want to participate in the study/do not give consent * Patients with a condition that prevents regional anesthesia * Patients with cognitive dysfunction who are unable to evaluate the NRS score and who cannot use PCA (Patient Controlled Analgesia Device) * History of hypersensitivity or allergy to local anesthetics * Patients with psychiatric disorders and those using psychiatric medications * Presence of hematological disease * Presence of oncological disease * Patients with serious major organ failure * Presence of multiple fractures * Patients with alcohol or drug addiction * Patients who have used analgesic drugs up to 12 hours before surgery * ASA IV-V patients * Morbidly obese patients

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Conditions

The condition(s) this trial relates to.

hip fracture

As listed by the trial registrant

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

Acute pain management Hip surgery

Contacts and locations

Locations

  • Samsun University, Samsun Training and Research Hospital

    Samsun, Ilkadım, Turkey (Türkiye)

More trials for these conditions

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