Clinical Trials Directory

Trials / Completed

CompletedNCT06685081

Dexmedetomidine for Improved Pain Relief and Recovery in Spine Surgery

Optimal-dose of Dexmedetomidine as Adjuvant to Epidural Local Anesthetic/Steroid Injectate to Improve Pain and Quality of Waking in Patients With Chronic Low Back Pain: A Randomized Case-control Study

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
150 (actual)
Sponsor
Menoufia University · Academic / Other
Sex
All
Age
35 Years – 75 Years
Healthy volunteers
Not accepted

Summary

Chronic low back pain (CLBP) is a prevalent condition causing significant pain, disability, and reduced quality of life. While various treatments like exercise, NSAIDs, and spinal manipulation are recommended, their effectiveness is limited. Epidural steroid injections can provide short-term relief but may not be cost-effective and have associated risks. Dexmedetomidine (DXM) is a selective α2-adrenergic agonist with analgesic properties. It has been used as an adjuvant to anesthetics and analgesics to enhance pain relief and reduce opioid consumption. Using DXM in conjunction with local anesthetics for regional blocks has shown promising results in improving analgesia and functional outcomes.

Conditions

Interventions

TypeNameDescription
DRUGDexmedetomidineDexmedetomidine was injected in dose of 0.25 µg/kg
DRUGDexmedetomidineDexmedetomidine was injected in dose of 0.5 µg/kg
DRUGDexmedetomidineDexmedetomidine was injected in dose of 0.75 µg/kg
DRUGDexmedetomidineDexmedetomidine was injected in dose of 1 µg/kg
DRUGlidocaine and triamcinolone2 ml of 1.5% lidocaine and 2 ml of triamcinolone was mixed and provided to all patients as epidural injection

Timeline

Start date
2024-07-01
Primary completion
2024-10-15
Completion
2024-11-01
First posted
2024-11-12
Last updated
2024-11-12

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT06685081. Inclusion in this directory is not an endorsement.