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Which pain block works best for broken hips?

NCT ID NCT06604806

Symptom relief Sponsor: Kanuni Sultan Suleyman Training and Research 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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 compared two types of nerve blocks—Quadroiliac Plane Block and PENG Block—for pain relief after femur fracture surgery. 52 adults were randomly assigned to receive one of the blocks. Researchers measured pain scores and how much opioid painkiller patients needed in the first 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 one block works better, it could improve pain control and reduce opioid use after hip fracture surgery.
What could go wrong
This is a small, completed study with only 52 patients. Results may not apply to everyone, and individual responses to nerve blocks vary.

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

52 people

The number who actually took part.

Started

Oct 2024

Finished

Sep 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 years and older

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 and their relatives have provided informed consent, * Patients aged 18 years or older undergoing femoral fracture surgery, * ASA score of I-III, * No history of bleeding diathesis, * No history of anticoagulant use that contraindicates block application according to guidelines, * No history of neuropathic diseases such as Diabetes Mellitus, * No known allergy to local anesthetics. Exclusion Criteria: * Lack of informed consent from the patient or their relatives, * Development of complications during the surgical procedure, * Need for revision surgery, * Patient\'s desire to withdraw from the study, * Patients under the age of 18, * ASA score of IV or higher, * Patients with a history of bleeding diathesis, * History of anticoagulant use that contraindicates block application according to guidelines, * Emergency surgeries, * History of allergy to local anesthetics, * History of neuropathic diseases, * Inability to comply with patient-controlled analgesia (PCA) systems.

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Conditions

The condition(s) this trial relates to.

agnosia bone fracture Femoral Fractures femoral neck fracture Pain

As listed by the trial registrant

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

Femur fractures

Contacts and locations

Locations

  • Health Science University İstanbul Kanuni Sultan Süleyman Education and Training Hospital

    Istanbul, Istanbul, 34303, Turkey (Türkiye)

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