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EvaluatIng Normal Values for traditionaL anorectaL fUnction paraMeters With aIr Charged aNd Solid State HRAM catheTErs ("ILLUMINATE" Study)
NCT06805240 · View on ClinicalTrials.gov ↗
Study Summary
The research study will be conducted to obtain baseline, or "normative" information to compare an air charged HRAM catheter to traditional solid catheter measures using the IAPWG standardized testing protocol and London classification.
Conditions Studied
Interventions
- DIAGNOSTIC_TEST Air Charged Catheter ARM Procedure
- DIAGNOSTIC_TEST Solid State Catheter ARM Procedure
Study Locations (3)
Georgia
- Augusta University Digestive Health Center — Augusta
Illinois
- Southwest Gastroenterology — New Lenox
Missouri
- Digestive Health Center of the Four States, LLC — Joplin
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 81 participants |
| Start Date | 2025-01-09 |
| Est. Completion | 2026-01 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06805240
The ClinicalTrials.gov registry entry for NCT06805240 describes a study currently listed as recruiting. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 81 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Laborie Medical Technologies, which has 30 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Healthy appearing as the primary indexed condition, and to 2 interventions — of which Air Charged Catheter ARM Procedure is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT06805240 reports 3 study locations spanning 3 distinct geographic areas — top geographies include Georgia, Illinois, Missouri. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT06805240 about?
NCT06805240 is a clinical study titled "EvaluatIng Normal Values for traditionaL anorectaL fUnction paraMeters With aIr Charged aNd Solid State HRAM catheTErs ("ILLUMINATE" Study)". The research study will be conducted to obtain baseline, or "normative" information to compare an air charged HRAM catheter to traditional solid catheter measures using the IAPWG standardized testing protocol and London classification.
What is the current status of trial NCT06805240?
This trial is currently recruiting. The enrollment target is 81 participants. The study started on 2025-01-09. Estimated completion is 2026-01.
What conditions does trial NCT06805240 study?
This clinical trial studies the following conditions: Healthy. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06805240?
The interventions under investigation include: Air Charged Catheter ARM Procedure (DIAGNOSTIC_TEST), Solid State Catheter ARM Procedure (DIAGNOSTIC_TEST). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06805240?
This trial is sponsored by Laborie Medical Technologies, which has 30 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06805240 being conducted?
This trial has 3 study locations across Georgia, Illinois, Missouri. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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