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New triple treatment offers hope for chronic back pain after surgery

NCT ID NCT07370233

Symptom relief Sponsor: Benha University 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 a combination of three procedures—spinal fixation, nerve heat treatment, and anti-inflammatory injections—for people with ongoing back and leg pain after disc surgery. 63 participants were split into two groups to see if the triple approach worked better than spinal fixation alone. The goal was to reduce pain and improve daily function.

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

Phase 2

Tests whether the treatment actually works, and watches for side effects, in a larger group.

Participants

63 people

The number who actually took part.

Started

Feb 2023

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

23 to 65 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: * Patients with persistent back pain after microdiscectomy (FBSS). * Failure of conservative treatment for at least six months. * Positive results on a diagnostic lumbar facet nerve block. Exclusion Criteria: * Spinal instability, fractures, or spondylolisthesis. * Severe psychiatric disorders. * Baseline ODI score higher than 60%. * Opioid users or history of adverse reactions to steroids.

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Conditions

The condition(s) this trial relates to.

spinal injury

As listed by the trial registrant

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

Spinal disk injury

Contacts and locations

Locations

  • Faculty of Medicine, Benha University

    Banhā, Qalyubia Governorate, 13511, Egypt