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Which anesthesia is safer for hip fracture surgery? new study investigates

NCT ID NCT07272226

Symptom relief Sponsor: Bursa Yuksek Ihtisas 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study compared two types of anesthesia for people having hip fracture surgery: a spinal block that numbs only one side and a nerve block in the lower back. Researchers wanted to see which method keeps blood pressure more stable and provides better pain control during surgery. The study included 50 adults aged 18 to 90. Results could help doctors choose the best anesthesia for each patient.

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 this study shows one method is better, it could help doctors choose the safest and most effective anesthesia for hip fracture surgery.
What could go wrong
This is a small, completed study with only 50 participants, so results may not apply to everyone. Both methods have risks like low blood pressure or allergic reactions.

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

50 people

The number who actually took part.

Started

Sep 2023

Finished

Dec 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: * Age between 18 and 90 years. * American Society of Anesthesiologists (ASA) classification I-IV. * Scheduled for femoral neck fracture surgery. * Provided informed consent to participate in the study. Exclusion Criteria: * History of allergy to local anesthetics. * Presence of coagulopathy or bleeding disorders. * Mental health disorders impairing consent or cooperation. * Allergy to medications used in the study protocol. * Presence of infection at the block site. * Body mass index (BMI) \> 30. * Preoperative or intraoperative conversion to general anesthesia. * Pregnant patients. * Severe spinal deformities preventing regional anesthesia application. * Refusal to participate in the study.

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Conditions

The condition(s) this trial relates to.

femoral neck fracture

As listed by the trial registrant

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

Femur neck fracture Lumbar plexus nerve block Spinal anesthesia

Contacts and locations

Locations

  • Healt Science University Bursa Yuksek Ihtisas Research and Education Hospital

    Bursa, Turkey (Türkiye)

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