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New pain block gets hip replacement patients walking faster?

NCT ID NCT06621849

Symptom relief Sponsor: Cairo University Source: ClinicalTrials.gov ↗

What the study statuses mean

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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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 two pain relief methods after hip replacement surgery: a nerve block (ESPB) versus morphine injected into the spine. The goal was to see which method helps patients walk 10 steps without support sooner. 70 adults aged 18-60 participated. The results could help improve recovery and reduce hospital stays.

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

Early phase 1

The earliest testing in people: a first look at safety, in a very small group.

Participants

70 people

The number who actually took part.

Started

Sep 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 to 60 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

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 18 to 60 yrs. old. * Both genders. * ASA I, II. * Body mass index between 20 to 30 kg per meter square. * Height between 160 cm and 180 cm Exclusion Criteria: * Patient refusal. * Age below 18 and above 60 yrs. old. * Uncooperative patients. * Known Allergy to the drugs enrolled in the study. * Body mass index \<30 or \< 20 kg per square meter * Any contraindication of spinal anaesthesia * ASA III, IV patients. * Emergency surgery. * Neuromuscular disorder interferes with sensations in the lower limbs. * Drug abuse or using any drug that modifies pain perception. * Any disability affecting walking capacity rather than the operating joint.

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Conditions

The condition(s) this trial relates to.

Pain, Postoperative

As listed by the trial registrant

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

Pain, postoperative

Contacts and locations

Locations

  • Faculty of Medicine- Cairo University

    Cairo, 11956, Egypt

More trials for these conditions

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