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New study aims to find best pain relief for hip surgery patients

NCT ID NCT07329829

Symptom relief Sponsor: Başakşehir Çam & Sakura City Hospital 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 looks at two different nerve-block methods to control pain after hip surgery. One group gets a standard block that numbs the hip joint, while the other gets an extra block for the thigh skin. The goal is to see which method reduces pain, lowers the need for pain medicine, and helps patients recover faster. 72 adults having hip surgery through a side incision will take part.

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

About 72 people

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

Started

Nov 2025

Expected to finish

Jul 2026

An estimate. End dates often move.

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 80 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 80 years * Patients scheduled for elective or trauma-related hip surgery performed through a lateral incision under spinal anesthesia * Patients receiving a preoperative ultrasound-guided Pericapsular Nerve Group (PENG) block or a PENG block combined with a Lateral Femoral Cutaneous Nerve (LFCN) block * American Society of Anesthesiologists (ASA) physical status I-III * Patients with full orientation and the ability to cooperate * Ability to understand the study procedures and provide written informed consent Exclusion Criteria: * Contraindications to regional anesthesia, including coagulopathy or local infection at the injection site * Presence of neuropathic disorders or conditions that may affect pain perception, including chronic analgesic use * Requirement for conversion to general anesthesia * Postoperative admission to the intensive care unit * Known allergy or hypersensitivity to opioids or local anesthetics * American Society of Anesthesiologists (ASA) physical status IV-V

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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.

Analgesia, postoperative Hip surgery (lateral incision) Hi̇P fracture Postoperative pain management Regional anesthesia success

Contacts and locations

Locations

  • Basaksehir Çam and Sakura City Hospital

    Istanbul, BASAKSEHİR, 34490, Turkey (Türkiye)

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