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New nerve block eases hip fracture pain before surgery

NCT ID NCT07194356

Symptom relief Sponsor: Dr. Lutfi Kirdar Kartal Training and Research Hospital 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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 a special nerve block called PENG can reduce pain when positioning patients with hip fractures for spinal anesthesia. Sixty adults having hip fracture surgery were randomly assigned to receive the block or not. The main goal was to see if the block made positioning less painful and improved pain control 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

60 people

The number who actually took part.

Started

Dec 2023

Finished

May 2024

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.

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: * Patients aged 18 to 90 years * ASA (American Society of Anesthesiologists) physical status classification I-III * Scheduled for proximal femoral nailing due to hip fracture * Able to provide informed consent (or consent provided by a legal representative) * Willingness to comply with study procedures and follow-up assessments Exclusion Criteria: * \- ASA physical status classification IV or V * Refusal to provide informed consent * Coagulopathy or current use of anticoagulant therapy contraindicating neuraxial block * Local infection at the injection site * Known allergy or hypersensitivity to local anesthetic agents * Cognitive impairment or inability to cooperate with study procedures * Severe psychiatric illness preventing reliable pain assessment * Previous surgery or deformity of the hip interfering with block performance * Pregnancy or lactation

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Conditions

The condition(s) this trial relates to.

agnosia hip fracture

As listed by the trial registrant

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

Elderly patients Hip fractures (icd-10 72.01-72.2) Postoperative pain management after total hip arthroplasty Regional anesthesia

Contacts and locations

Locations

  • Facility Name: Kartal Dr. Lütfi Kırdar City Hospital, University of Health Sciences

    Istanbul, 34890, Turkey (Türkiye)

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