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Recruiting NCT06200961

NCT06200961 Trans-nasal Endoscopy for Bariatric Patients

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Clinical Trial Summary
NCT ID NCT06200961
Status Recruiting
Phase —
Sponsor Christopher C. Thompson, MD, MSc
Condition Obesity
Study Type INTERVENTIONAL
Enrollment 100 participants
Start Date 2026-04-20
Primary Completion 2027-12

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 90 Years
Study Type INTERVENTIONAL
Interventions
Transnasal EndoscopyEsophagogastroduodenoscopy

Eligibility Fast-Check

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What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 100 participants in total. It began in 2026-04-20 with a primary completion date of 2027-12.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This study plans to learn if the EvoEndo Endoscopy system can be used to evaluate, provide and follow up care for upper gastrointestinal tract diseases in the bariatric population. The smallest current scope available for such a technique is an adult transnasal endoscope with a larger diameter, a pulmonary bronchoscope or Ear Nose and Throat (ENT) laryngoscope. This study is evaluating a newly Food and Drug Administration (FDA) cleared ultra-slim, single-use, endoscope specifically designed for transnasal endoscopy to evaluate its use in adult upper tract gastrointestinal diseases. If such a technique is successful it could improve the safety, cost, and access of endoscopic care for patients in need of an endoscopic evaluation for a bariatric medical condition.

Eligibility Criteria

Inclusion Criteria: 1. Patient 18 years of age and less than 90 years of age with clinically referred for esophagoscopy, gastroscopy, or esophagogastroduodenoscopy (EGD) 2. Cared for in metabolic and bariatric clinic Exclusion Criteria: 1. Patient \<18 years of age 2. Medically contraindicated to perform EGD or TNE 3. Inability to provide informed consent

Contact & Investigator

Central Contact

Michele B Ryan, MS

✉ mryan@bwh.harvard.edu

📞 617-525-8266

Principal Investigator

Christopher C. Thompson, MD, MSc

PRINCIPAL INVESTIGATOR

Brigham and Womens Hospital

Frequently Asked Questions

Who can join the NCT06200961 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 90 Years, studying Obesity. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06200961 currently recruiting?

Yes, NCT06200961 is actively recruiting participants. Contact the research team at mryan@bwh.harvard.edu for enrollment information.

Where is the NCT06200961 trial being conducted?

This trial is being conducted at Boston, United States.

Who is sponsoring the NCT06200961 clinical trial?

NCT06200961 is sponsored by Christopher C. Thompson, MD, MSc. The principal investigator is Christopher C. Thompson, MD, MSc at Brigham and Womens Hospital. The trial plans to enroll 100 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: November 2026  ·  Data Methodology