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Spine surgery pain study seeks better recovery

NCT ID NCT07245524

Symptom relief Sponsor: A.O.U. Città della Salute e della Scienza 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 looked at two different methods to control pain after spinal fusion surgery: injecting morphine near the spine or using a nerve block. The goal was to see which approach works better for pain relief and reduces the need for extra painkillers. Fifty adults having spine surgery took part, and their pain levels and side effects were tracked for 24 hours after the operation.

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

50 people

The number who actually took part.

Started

Aug 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.

Who is studied

Patients with presenting surgical indication for thoracolumbar spinal fusion with posterior access. The patients enrolled are being treated at the CTO (Trauma and Orthopedic Center) hospital in Turin.

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: * Age \>=18 years * Patients with surgical indication for thoracolumbar spinal fusion with posterior access. * ASA I, II, III Exclusion Criteria: * Patient refusal * Emergency surgery * Chronic use (\>12 weeks) of opioids in the preoperative period * Drug addiction * Contraindication to drugs contained in the protocol * Contraindications to performing a subarachnoid puncture or fascial block

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As listed by the trial registrant

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

Erector spina plan block Intrathecal anesthesia Locoregional anaesthesia Multimodal general anesthesia Spine fusion

Contacts and locations

Locations

  • Centro Traumatologico Ortopedico (CTO) - AOU Città della Salute e della Scienza University Hospital

    Torino, To, 10126, Italy

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