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Adjunctive Wet Cupping for Acute Non-Specific Low Back Pain

StatusCompleted
PhaseNot applicable
Started
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Record History

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  1. Minor Eligibility criteria expanded, about 14 words
  2. Minor 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
This prospective randomized controlled trial evaluated the effectiveness and safety of adjunctive wet cupping therapy combined with standard pharmacological treatment in adults presenting to the emergency department with acute non-specific low back pain. A total of 80 adult patients were randomly assigned to receive either wet cupping therapy plus intravenous dexketoprofen or intravenous dexketoprofen alone. Pain intensity was assessed using the Visual Analogue Scale (VAS) at baseline and at 10, 20, and 30 minutes after treatment, as well as at 24 hours. Secondary outcomes included the need for rescue analgesia, analgesic consumption during the first 24 hours after discharge, patient satisfaction, and treatment-related adverse events. The study was designed to determine whether adding wet cupping therapy to standard pharmacological treatment provides additional pain relief and improves short-term clinical outcomes in patients with acute non-specific low back pain.
Trial Details
NCT Number NCT07837596
Lead Sponsor Ataturk University
Conditions
(from sponsor)
Acute Non-specific Low Back Pain
Related terms Agnosia, Emergencies
Enrollment 80 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov