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NCT06676488 · ClinicalTrials.gov registry record · NA
A Randomized Crossover Trial of Bright Light Therapy in Irritable Bowel Syndrome
A NA study of Irritable Bowel Syndrome (IBS) and Circadian Misalignment, sponsored by Medical University of South Carolina.
- Recruiting
- Registry status
- NA
- Development phase
- 30
- Enrollment target
- 1
- Study location
NCT06676488 is a NA study of Irritable Bowel Syndrome (IBS) and Circadian Misalignment that is actively recruiting participants, run by Medical University of South Carolina. The registered enrollment target is 30 participants, below the 1,183-participant average among 5 other Irritable Bowel Syndrome (IBS) trials with a reported enrollment target (97% lower). The trial reports 1 study location across 1 state.
The verdict
NCT06676488, a NA study of Irritable Bowel Syndrome (IBS) and Circadian Misalignment, is actively recruiting participants, sponsored by Medical University of South Carolina.
- RECRUITING
- Registry status
- NA
- Development phase
- 30 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this research study is to assess whether morning bright light therapy (BLT) using a wearable device called a Re-Timer could potentially improve Irritable Bowel Syndrome (IBS) symptoms and decrease intestinal permeability (leaky gut). Morning bright light therapy will be administrated through a safe-wearable glasses device called a Re-Timer. The Re-Timer glasses are lightweight and deliver blue-green light at 500nm, mimicking exposure to natural light.
Conditions Studied
Interventions
- DEVICE Re-Timer glasses
- DEVICE Placebo Device
Study Locations (1)
South Carolina
- Medical University of South Carolina - Charleston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 30 participants |
| Start Date | 2025-06-11 |
| Est. Completion | 2026-03-31 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06676488
The ClinicalTrials.gov registry entry for NCT06676488 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 30 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 1,183-participant average among 5 other Irritable Bowel Syndrome (IBS) trials with a reported enrollment target (97% lower). The listed sponsor is Medical University of South Carolina, which has 755 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Irritable Bowel Syndrome (IBS) appearing as the primary indexed condition, and to 2 interventions - of which Re-Timer glasses is the first listed.
NCT06676488 reports 1 study location spanning 1 distinct geographic area - top geographies include South Carolina.
Frequently Asked Questions
What is clinical trial NCT06676488 about?
NCT06676488 is a clinical study titled "A Randomized Crossover Trial of Bright Light Therapy in Irritable Bowel Syndrome". The purpose of this research study is to assess whether morning bright light therapy (BLT) using a wearable device called a Re-Timer could potentially improve Irritable Bowel Syndrome (IBS) symptoms and decrease intestinal permeability (leaky gut). Morning bright light therapy will be administrated ...
What is the current status of trial NCT06676488?
This trial is currently recruiting. It is a NA study. The enrollment target is 30 participants. The study started on 2025-06-11. Estimated completion is 2026-03-31.
What conditions does trial NCT06676488 study?
This clinical trial studies the following conditions: Irritable Bowel Syndrome (IBS), Circadian Misalignment.
What interventions are being tested in trial NCT06676488?
The interventions under investigation include: Re-Timer glasses (DEVICE), Placebo Device (DEVICE).
Who is sponsoring clinical trial NCT06676488?
This trial is sponsored by Medical University of South Carolina, which has 755 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06676488 being conducted?
This trial has 1 study location across South Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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