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Pain Intervention With Needling: Pilot Of Integrated Neuromodulation Techniques

Study acronym: PINPOINT
StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗

Record History

  1. 2 versions Re-verified since Mar 11, 2026, no change to tracked fieldsv5-v6
  2. Trial status: Not Yet Recruiting to Recruiting
    • Start date changed from estimate of Dec 2025 to Oct 23, 2025
    • Site details revised
    v4
  3. Start date: Oct 2025 to Dec 2025v3
  4. Start date: Aug 2025 to Oct 2025v2
  5. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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 study will be conducted on site in Galveston, Texas, United States. Study-related assessments and procedures will be performed at the designated clinical study site by qualified study personnel in accordance with the study protocol and applicable regulatory requirements. The study's purpose is to determine the effects of three different dry needling sessions on pain and quality of life for those with chronic low back pain. Dry needling is a therapeutic procedure in which a very thin, monofilament needle is inserted through the skin to reach a target tissue like a muscle to help reduce pain, improve muscle activation, and increase blood flow. Dry needling has also been shown to improve nervous system function.
Trial Details
NCT Number NCT07112404
Lead Sponsor The University of Texas Medical Branch, Galveston
Collaborators: National Institute of Neurological Disorders and Stroke (NINDS)
Conditions
(from sponsor)		 Pain, Back Pain, Lower Back Pain, Quality of Life
Related terms Back Pain, Low Back Pain, Pain
Enrollment 42 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov