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Effectiveness of Thoracolumbar Fascia Mobilization and Ultrasound-Guided 5% Dextrose Injection in Chronic Low Back Pain

StatusRecruiting
PhaseNot applicable
Started
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Record History

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  1. Re-verified, no change to tracked fieldsv3
  2. Start date: May 20, 2025 to Nov 1, 2025v2 Show 6 more changesShow less
    • Primary completion date: Nov 20, 2025 to Apr 1, 2026
    • Study completion date: Feb 20, 2026 to Jul 1, 2026
    • Interventions: 5% Dextrose (Drug), Myofascial Release (Procedure) to 5% dextrose injection (Drug), Myofascial Release (Procedure)
    • Secondary endpoints revised (3)
    • Study description expanded, about 511 words
    • Study title shortened, about 7 words
  3. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The aim of this study is to investigate the effects of thoracolumbar fascia mobilization and ultrasound-guided thoracolumbar interfascial 5% dextrose injection on pain, range of motion, disability, quality of life, proprioception, and fascial thickness and echogenicity in patients with nonspecific chronic low back pain. -Primary Objective: The primary objective is to evaluate the effects of these interventions on pain, functional status and range of motion. -Secondary Objective: The secondary objective is to assess the long-term effects on quality of life, proprioception, fascial thickness, and echogenicity.
Trial Details
NCT Number NCT07241559
Lead Sponsor Ankara City Hospital Bilkent
Collaborators: Ankara Training and Research Hospital
Conditions
(from sponsor)		 Chronic Low Back Pain
Enrollment 75 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov