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New combo approach may ease pain after knee surgery

NCT ID NCT07257757

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 completed study looked at whether adding a continuous nerve block (fascia iliaca compartment block) to a standard joint injection can better control pain after total knee replacement. Researchers reviewed records of 60 patients to compare pain scores and satisfaction. 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
fascia iliaca compartment block (nerve block) plus intra-articular injection
What this could lead to
If effective, this combination approach could offer better pain control after knee replacement surgery, reducing the need for strong painkillers.
What could go wrong
This is a small, retrospective study (60 patients) that only looks back at records, not a controlled trial. Results may not apply to all patients.

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.

Participants

60 people

The number who actually took part.

Started

Jun 2024

Finished

Jun 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.

Who is studied

Patients who underwent unilateral total knee arthroplasty at the Orthopedics and Traumatology Clinic of Kırıkkale University Faculty of Medicine Hospital and received postoperative analgesia using different methods

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: * Total knee arthroplasty cases with or without continuous fascia iliaca compartment block * Patients with ASA criteria 1-2-3 Exclusion Criteria: * Patients whose records cannot be accessed * Patients with ASA criteria 4-5

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Conditions

The condition(s) this trial relates to.

Hemorrhage Pain Pain, Postoperative Patient Satisfaction

As listed by the trial registrant

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

Contacts and locations

Locations

  • Kırıkkale University

    Kirikkale, 71100, Turkey (Türkiye)

More trials for these conditions

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