New study tests Opioid-Free pain control for back surgery patients
NCT ID NCT06725680
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study compared two types of nerve blocks (retrolaminar block and erector spinae plane block) for pain control after lumbar discectomy surgery. The goal was to see which block better reduces the need for opioid painkillers and speeds up recovery. 90 adults undergoing elective back surgery were randomly assigned to receive one of the two blocks. Researchers measured how long it took for patients to need rescue pain medication and how quickly they recovered from anesthesia.
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 (retrolaminar block or erector spinae plane block)
- What this could lead to
- If one block works better, it could offer a way to manage pain after back surgery without relying on opioids, leading to faster recovery and fewer side effects.
- What could go wrong
- This is a small, completed trial with only 90 participants. The results may not apply to all patients or surgeries, and nerve blocks carry risks like infection or nerve damage.
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
-
90 people
The number who actually took part.
- Started
-
Dec 2024
- Finished
-
Oct 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 65 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 Hide 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 from 18 to 65 years. * Both sexes. * American Society of Anesthesiology (ASA) physical status I-II. * Undergoing elective posterior lumbar discectomy under general anesthesia. Exclusion Criteria: * Body mass index (BMI) \>35 kg/m2. * Patients with disturbed mental status. * Allergies to the drugs used in the study. * Local infection at the puncture site. * Cardiac insufficiency. * Renal insufficiency. * Coagulopathy. * Chronic opioid use.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Enhanced recovery are added.
Genom att skicka in godkänner du våra Användarvillkor
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Tanta University
Tanta, El-Gharbia, 31527, Egypt
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- A nerve block that spares arm movement tested for shoulder surgery pain
- Could a nerve block replace opioids for severe belly pain in the ER?
- Sinus surgery without opioids: can dexmedetomidine do the job?
- Could lying a certain way after a nerve block double its pain relief?
- Can a targeted nerve block cut opioid use after spine surgery?
- Can surgery pain be managed without opioids?