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New injection may cut opioid use after broken hip surgery

NCT ID NCT07009782

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 tested whether a Quadroiliac Plane (QIP) block, a numbing injection near the hip, can reduce pain and opioid use after femur fracture surgery. Thirty adults were randomly assigned to receive either the QIP block or standard care. Researchers measured pain scores and fentanyl use over 24 hours. The goal is to find a safer, more effective way to manage post-surgery pain.

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 it works, this could offer a better way to control pain after femur fracture surgery, reducing the need for strong opioids.
What could go wrong
This is a small, completed trial with only 30 participants. The results may not apply to everyone, and the block carries risks like any injection near nerves.

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

30 people

The number who actually took part.

Started

Jun 2025

Finished

Oct 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: * Adults aged 18 years and older * Scheduled for partial hip arthroplasty due to femur fracture * ASA physical status classification I to III * No contraindications to regional anesthesia or study medications * Capable of understanding and using patient-controlled analgesia (PCA) * Provided written informed consent Exclusion Criteria: * ASA classification IV or higher * History of bleeding disorders or use of anticoagulant therapy * Known allergy to local anesthetics * Presence of neuropathic pain disorders * Undergoing emergency surgery * Unable to operate PCA device * Declined to participate or refused consent

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Conditions

The condition(s) this trial relates to.

Femoral Fractures femoral neck fracture Pain, Postoperative

As listed by the trial registrant

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

Femur fracture

Contacts and locations

Locations

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

    Istanbul, Istanbul, 34303, Turkey (Türkiye)

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