Actively Recruiting
Impact of Per Oral Pyloromyotomy (POP) on Glycemic Control in Diabetes
Led by Matthew Allemang · Updated on 2025-07-24
40
Participants Needed
1
Research Sites
229 weeks
Total Duration
On this page
Sponsors
M
Matthew Allemang
Lead Sponsor
S
Society of American Gastrointestinal and Endoscopic Surgeons
Collaborating Sponsor
AI-Summary
What this Trial Is About
This study will assess changes in glycemic control in 40 patients with diabetes who undergo per-oral pyloromyotomy (POP) for medically refractory gastroparesis.
CONDITIONS
Official Title
Impact of Per Oral Pyloromyotomy (POP) on Glycemic Control in Diabetes
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients 18 years of age and older
- Patients with gastroparesis with an average HbA1c greater than 7.5% over the past 3 months
- Patients diagnosed with gastroparesis confirmed by delayed gastric emptying via wireless motility capsule study or nuclear gastric emptying study, with no gastric obstruction
- Patients able to complete all study requirements
You will not qualify if you...
- Patients younger than 18 years of age
- Patients with gastroparesis with an average HbA1c less than 7.5% over the past 3 months
- Patients unable or unwilling to complete the study requirements
- Patients unable or unwilling to wear a continuous glucose monitor (CGM) sensor
- Patients who use insulin pumps
- Patients who already use a continuous glucose monitor (CGM)
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Cleveland Clinic Foundation
Cleveland, Ohio, United States, 44195
Actively Recruiting
Research Team
D
Deanne Nash, RN
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
1
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