NCT05039424

Endoscopic Myotomy of the Pylorus To Improve Emptying and Symptoms Trial

Name: Clinical Trial NCT05039424
Creator: The Cleveland Clinic
Keywords: Gastroparesis, Endoscopic per-oral pyloromyotomy (POP), procedure, clinical trial, United States of America

A Randomized, Sham-controlled Trial: Endoscopic Myotomy of the Pylorus To Improve Emptying and Symptoms (EMPTIES)

The Cleveland Clinic·ClinicalTrials.gov·procedureRecruiting

View on ClinicalTrials.gov →

Study focus

Disease/Condition: Gastroparesis
Drug/Device/Intervention: Endoscopic per-oral pyloromyotomy (POP)
Study type: Interventional
Intervention type: procedure

Sponsor & location

Primary sponsor: The Cleveland Clinic
Location: Cleveland, United States of America

Timeline & enrollment

Phase: N/A
Start date: Feb 23, 2022
End date: Jul 01, 2026
Enrollment: 100 participants

Primary outcome

Gastroparesis Cardinal Symptom Index (GCSI)

Summary

A randomized clinical trial comparing endoscopic per-oral pyloromyotomy (POP) versus a control sham intervention (diagnostic esophagogastroduodenoscopy (EGD) without pyloric disruption) in patients with medically refractory gastroparesis.

ICD-10 classifications

Attention to gastrostomyGastrostomy statusOther gastritisGastritis, unspecifiedGastric diverticulum

Data source

Registry: ClinicalTrials.gov
Trial ID: NCT05039424
Type: Non-Device Trial

About this record

Access comprehensive clinical trial information for NCT05039424 through Pure Global AI's free database. This phase not specified trial is sponsored by The Cleveland Clinic and is currently Recruiting. The study focuses on Gastroparesis. Target enrollment is 100 participants.

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