Actively Recruiting

Age: 6Months - 90Years
All Genders
Healthy Volunteers
NCT02165059

GI Neuromuscular Pathology Prospective Registry

Led by Indiana University · Updated on 2024-10-08

300

Participants Needed

1

Research Sites

626 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

In this research study, biopsy samples will be collected to provide more insight into the underlying cause of the motility disorders, help direct further investigation into the cause of the underlying condition, provide future prognosis and predict response to gastric electrical stimulation (GES).

CONDITIONS

Official Title

GI Neuromuscular Pathology Prospective Registry

Who Can Participate

Age: 6Months - 90Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients undergoing surgical full-thickness biopsy of the stomach and/or proximal jejunum for clinical evaluation of GI neuromuscular disorder.
  • Patients undergoing esophagectomy, sleeve gastrectomy for obesity, or Roux-en-Y gastric bypass.
  • Patients undergoing Whipple surgery.
  • Patients undergoing transplant surgery.
  • Patients who are organ donors and undergoing surgery.
Not Eligible

You will not qualify if you...

  • Contraindication for surgical full-thickness biopsy for any reason.
  • Severe cardiovascular, renal, pulmonary, or liver disease.
  • Significant coagulopathy.
  • Non-ambulatory patients, including bed-ridden or nursing home residents.
  • Pregnant individuals.
  • Unable to give informed consent.
  • Prisoners.
  • Prior diagnosis of gastroparesis (control group).
  • Prior diagnosis of chronic intestinal pseudo-obstruction (control group).

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Indiana University Hosptial

Indianapolis, Indiana, United States, 46202

Actively Recruiting

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Research Team

M

Maureen Schilling

CONTACT

L

Lainna Cohen

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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