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Clinical Trials/NCT06908551
NCT06908551
Not yet recruiting
Not Applicable

Pylorus Distensibility Measurement in Overweight and Obese (BMI 27-40) Patients

BariaTek Medical0 sites40 target enrollmentStarted: April 1, 2025Last updated:

Overview

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
40
Primary Endpoint
Calculation of pylorus Cross Sectional Area

Overview

Brief Summary

The present study aims at characterizing the pylorus functionality in overweight and obese patients (BMI 27-40) using a systematic measurement approach by using an impedance planimetry technology.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
20 Years to 60 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Male and female subjects aged between 20 and 60 years inclusive
  • A BMI between 27.0 and 40.0 kg/m2
  • Willing and able to provide written informed consent
  • Willing and able to comply with the study procedures

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Calculation of pylorus Cross Sectional Area

Time Frame: Baseline

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Industry
Responsible Party
Sponsor

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