drugset / Trial / NCT06617065

Exploring Long-term Pain Relief with 5% Dextrose Added to Local Anesthetic

NCT06617065

Active not recruiting 70 enrolled The Seekers Centre
NaSingle-groupOpen-labelTreatment

Summary

The goal of this single-arm, non-randomized, open-label trial is to determine whether adding a 5% dextrose solution to a local anesthetic can improve outcomes in patients with chronic non-cancer pain. The main question we aim to answer is whether adding a low-concentration (5%) dextrose solution to local anesthetics increases the effectiveness of trigger point injections and/or peripheral nerve blockade in the treatment of chronic non-cancer pain. Researchers will compare the outcomes of adding 5% dextrose to the usual local anesthetic solution with the outcomes of using the local anesthetic alone to determine if injection therapy is more effective when dextrose is added. Participants will: * Attend their scheduled injection treatments every two (2) weeks for a total of six (6) visits. * Complete a demographic form at the first visit, and the usual pre-visit questionnaires (the Waiting Room Form and the Brief Pain Inventory (BPI)) at every visit, as well as four (4) weeks after the sixth visit (approximately 16 weeks from the study start date). They will also need to complete two short questionnaires-the Patient Health Questionnaire (PHQ-9) and the Patient Global Impression of Change (PGIC)-at the specified intervals. * Complete all forms, which will be securely emailed to them.

Timeline

Start
2024-09-03
Primary completion
2025-01-30
Completion
2025-02-28

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Dextrose Unknown 1 ml Other
Subject Dextrose Unknown 50 % Other
Background Bupivacaine Other / unclassified 0.25 %
Background Lidocaine Other / unclassified 0.5 %
Background Lidocaine Other / unclassified 2 %
Background Procaine Small molecule 1 %
Background Ropivacaine Other / unclassified 0.3 %

Indications