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Acupuncture Therapy for Pediatric Disorders of Gut-Brain Interaction

StatusRecruiting
PhaseNot applicable
Started
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Record History

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  1. Notable Primary endpoint(s) modified
    • Secondary endpoints: 5 to 6
    v5
  2. Minor 2 versions Re-verified since May 12, 2026, no change to tracked fieldsv3-v4
  3. Minor Primary completion pushed from Oct 1, 2027 to Dec 2027
    • Study completion date: Jan 1, 2028 to Jan 2028
    • Eligibility criteria shortened, about 58 words
    • Secondary endpoints: details revised at 5 of 5 entries
    v2
  4. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
Disorders of Gut-Brain Interactions (DGBIs) significantly impact children globally, leading to reduced quality of life and increased healthcare utilization. Despite their prevalence, effective treatments for pediatric DGBIs remain limited. Acupuncture, though commonly used in clinical practice and supported by adult data, lacks robust empirical evidence in pediatric populations. This study addresses this critical gap. The primary objective is to assess the efficacy of acupuncture in reducing symptom severity in pediatric patients with DGBIs. Key secondary objectives include evaluating improvements in quality of life, functional disability, and mental health outcomes. This is a parallel-group, randomized, placebo sham-controlled, participant-blind clinical trial. The study is being conducted in an outpatient pediatric referral center. A total of 96 participants, aged 8-17 years, meeting eligibility criteria for DGBIs will be enrolled. Participants must be medically stable and meet protocol-defined inclusion/exclusion criteria. Participants will be randomly assigned to receive either acupuncture or sham acupuncture, alongside standard care. Treatments will occur over a predefined protocol period. Data will be collected at baseline, during treatment, and at specified post-treatment intervals. The primary outcomes will evaluate changes in pain intensity and frequency. Secondary outcomes will include assessments of pain resolution, quality of life, functional disability, and mental health. Statistical analyses will employ rigorous methodologies to ensure reliability and validity of findings.
Trial Details
NCT Number NCT07435610
Lead Sponsor Children's Hospital of Orange County
Conditions
(from sponsor)
Disorders of Gut-brain Interaction
Enrollment 96 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov