Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

RECRUITING NA

Safety and Effectiveness of Endoscopic Intestinal Re-Cellularization Therapy in Individuals With Type II Diabetes

NCT06267391 · View on ClinicalTrials.gov ↗

Study Summary

This study is designed to evaluate the safety and effectiveness of endoscopic intestinal re-cellularization therapy in individuals with type 2 diabetes (T2D) inadequately controlled on non-insulin glucose-lowering medications.

Interventions

  • DEVICE ReCET Treatment
  • DEVICE Sham Procedure

Study Locations (20)

Florida

  • Velocity Clinical Research, Hallandale Beach — Hallandale
  • Mayo Clinic — Jacksonville
  • Universal Axon Clinical Research LLC — Miami
  • University of Miami — Miami
  • Quantum Clinical Research — Miami Beach
  • West Orange Endocrinology — Ocoee
  • Advent Health — Orlando
  • Orlando Health — Orlando
  • Health Synergy Clinical Research — West Palm Beach

California

  • Velocity Clinical Research, Gardena — Gardena
  • Cedars-Sinai Medical Center — Los Angeles
  • UCLA — Los Angeles
  • Hoag Memorial Hospital Presbyterian - Digestive Health Institute — Newport Beach
  • Velocity Clinical Research, Panorama City — Panorama City

Alabama

  • University of Alabama — Birmingham
  • Central Alabama Research — Birmingham

Iowa

  • Heartland Medical Research, Inc. — Clive
  • Iowa Diabetes and Endocrinology Research Center — West Des Moines

Illinois

  • NorthShore University Health System — Evanston

Maryland

  • John Hopkins — Baltimore

Trial Details

FieldValue
Enrollment Target 264 participants
Start Date 2024-05-01
Est. Completion 2026-10-01
Phase NA

Sponsor

Endogenex

1 total trials

Interested in This Trial?

Always speak with your doctor before enrolling in a clinical trial.

Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06267391

The ClinicalTrials.gov registry entry for NCT06267391 describes a study currently listed as recruiting. It is categorized as NA, 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 264 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Endogenex, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 5 conditions, with Diabetes appearing as the primary indexed condition, and to 2 interventions — of which ReCET Treatment 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: NCT06267391 reports 20 study locations spanning 6 distinct geographic areas — top geographies include Florida, California, Alabama. 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 NCT06267391 about?

NCT06267391 is a clinical study titled "Safety and Effectiveness of Endoscopic Intestinal Re-Cellularization Therapy in Individuals With Type II Diabetes". This study is designed to evaluate the safety and effectiveness of endoscopic intestinal re-cellularization therapy in individuals with type 2 diabetes (T2D) inadequately controlled on non-insulin glucose-lowering medications.

What is the current status of trial NCT06267391?

This trial is currently recruiting. It is a NA study. The enrollment target is 264 participants. The study started on 2024-05-01. Estimated completion is 2026-10-01.

What conditions does trial NCT06267391 study?

This clinical trial studies the following conditions: Diabetes, Diabetes Mellitus, Type 2, Type 2 Diabetes, Type 2 Diabetes Mellitus, Type2diabetes. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06267391?

The interventions under investigation include: ReCET Treatment (DEVICE), Sham Procedure (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06267391?

This trial is sponsored by Endogenex, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06267391 being conducted?

This trial has 20 study locations across Alabama, California, Florida, Illinois, Iowa. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial