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New pain block study aims to get hip surgery patients moving faster

NCT ID NCT07442721

Symptom relief Sponsor: Fayoum University Hospital Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 compares two types of nerve blocks—sacral erector spinae plane block and pericapsular nerve group block—for pain relief after hip hemiarthroplasty. Eighty adults aged 50-90 with a hip fracture will receive one of the blocks before surgery. Researchers will measure pain scores at rest and during movement over 24 hours to see which block provides better pain control while preserving leg strength for early walking.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
nerve block (sacral erector spinae plane block or pericapsular nerve group block)
What this could lead to
If successful, this could identify a better pain-blocking technique for hip surgery, reducing opioid use and speeding recovery.
What could go wrong
This is a small, early-stage trial with only 80 participants. Results may not apply to all patients, and the blocks may not work as well in practice.

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 80 people

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

Started

Feb 2026

Expected to finish

Aug 2027

An estimate. End dates often move.

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

50 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 with ages from 50 to 90 years of either gender, with diagnosis of intracapsular neck of femur fracture scheduled for elective hip hemiarthroplasty • Patients with an American Society of Anesthesiologists (ASA) physical status I to III. Exclusion Criteria: * • Patient refusal. * Allergy to local anesthetics and patient with infection at the injection site of block * Patient with contraindication to spinal anesthesia. * Coagulopathy as INR≥1.5 or platelets ≤80\*103 / microliter) * Patients with body mass index\>35 kg / m2 * Patients with peripheral neuropathy or diabetic neuropathy * Patients receiving opioids for chronic analgesic therapy (cancer, addiction). * Cognitive impairment preventing pain scoring. * Chronic renal failure requiring dose modification. * Bilateral hip fracture or previous ipsilateral hip surgery

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Conditions

The condition(s) this trial relates to.

femoral neck fracture hip fracture Pain, Postoperative

As listed by the trial registrant

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

Femoral neck fractures Hip arthroplasty Hip fracture surgeries Postoperative pain

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Fayoum University hospita

    RECRUITING

    El Fayoum Qesm, Faiyum Governorate, 63514, Egypt

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