Cooperative Group for Clinical Research in G-POEM (POP), Jiangsu, China

Not Applicable

• Conditions: Gastric Peroral Endoscopic Pyloromyotomy (G-POEM)
• Interventions: Drug: Esomeprazole + Mosapride; Procedure: Gastric peroral endoscopic pyloromyotomy (G-POEM)

• Registration Number: NCT03040817
• Lead Sponsor: Zhongda Hospital

Brief Summary

Diabetic gastroparesis, postsurgical gastroparesis, idiopathic gastroparesis and primary pyloric stenosis are debilitating gastrointestinal motility disorder. However, there is limited medical therapeutic options for these diseases. Gastric peroral endoscopic pyloromyotomy (G-POEM) is an emerging novel endoscopic technique which is reported as a minimally invasive therapy. But so far, the efficacy and safety of G-POEM on these diseases are rarely explored. So, there is a cooperative group composed of five clinical centers for clinical research in G-POEM.

Detailed Description

Participants are randomly devided into 'G-POEM group' and 'Esomeprazole+Mosapride group'. In G-POEM group, each participant receives G-POEM treatment. In Esomeprazole+Mosapride group, each participant receives Nexium 40mg bid + Mosapride Citrate Tablets 5mg tid. The whole outcome measure time fram is up to two years. Outcome evaluations include: gastric emptying imaging, gastric antrum volume, gastric emptying time, gastroparesis cardinal symptoms index and gastroesophageal reflux disease questionnaire. All the outcomes are assessed at different time points (from baseline to 6 months, 12months and 24months).

Study Timeline

• Study First Submitted: 2017-01-31
• Study First Submitted QC: 2017-01-31
• Study First Posted: 2017-02-02
• Status Verified: 2017-08
• Last Update Submitted: 2017-08-26
• Last Update Posted: 2017-08-29
• Study Start: 2017-09-01
• Primary Completion: 2019-08-16
• Study Completion: 2019-12-16

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 50

Inclusion Criteria

1. Age between 16 to 80 years old
2. Full sufficiency in literacy
3. Be off proton pump inhibitor, antacids and prokinetics ≥ 2 weeks
4. Refractory gastroesophageal reflux disease induced by postsurgical gastroparesis

Exclusion Criteria

1. Severe heart, lung, and cerebrovascular disease
2. Severe hematopoietic system disease
3. Abnormal blood coagulation function
4. Oropharyngeal abnormalities
5. Severe spine malformation
6. In pregnancy and lactation at present, or plan to become pregnant within 2 years
7. Severe inflammation or huge ulcers in stomach
8. Mental and psychological disorder

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Esomeprazole + Mosapride	Esomeprazole + Mosapride	Each participant receive Esomeprazole+ Mosapride. The dosages are：Nexium 40mg bid， Mosapride Citrate Tablets 5mg tid.
G-POEM	Gastric peroral endoscopic pyloromyotomy (G-POEM)	Each participant receive gastric peroral endoscopic pyloromyotomy (G-POEM).

Primary Outcome Measures

Name	Time	Method
Change from Baseline in Gastric Emptying Imaging at 6 months.	From baseline to 6 months.	Each participant will receive gastric emptying imaging measurement both at baseline and 6 months.
Change from Baseline in Gastric Emptying Time at 6 months.	From baseline to 6 months.	Each participant will receive gastric emptying time measurement both at baseline and 6 months.
Change from Baseline in Gastric Antrum Volume at 6 months.	From baseline to 6 months.	Each participant will receive gastric antrum volume measurement both at baseline and 6 months.
Change from Baseline in Gastroparesis Cardinal Symptoms Index at 12 months.	From baseline to 12 months.	Each participant will receive gastroparesis cardinal symptoms index evaluation both at baseline and 12 months.
Change from Baseline in Gastroesophageal Reflux Disease Questionnaire at 6 months.	From baseline to 6 months.	Each participant will receive gastroesophageal reflux disease questionnaire evaluation both at baseline and 6 months.
Change from Baseline in Gastroesophageal Reflux Disease Questionnaire at 24 months.	From baseline to 24 months.	Each participant will receive gastroesophageal reflux disease questionnaire evaluation both at baseline and 24 months.
Change from Baseline in Gastric Emptying Imaging at 12 months.	From baseline to 12 months.	Each participant will receive gastric emptying imaging measurement both at baseline and 12 months.
Change from Baseline in Gastric Emptying Imaging at 24 months.	From baseline to 24 months.	Each participant will receive gastric emptying imaging measurement both at baseline and 24 months.
Change from Baseline in Gastroparesis Cardinal Symptoms Index at 6 months.	From baseline to 6 months.	Each participant will receive gastroparesis cardinal symptoms index evaluation both at baseline and 6 months.
Change from Baseline in Gastroesophageal Reflux Disease Questionnaire at 12 months.	From baseline to 12 months.	Each participant will receive gastroesophageal reflux disease questionnaire evaluation both at baseline and 12 months.
Change from Baseline in Gastric Emptying Time at 24 months.	From baseline to 24 months.	Each participant will receive gastric emptying time measurement both at baseline and 24 months.
Change from Baseline in Gastric Antrum Volume at 12 months.	From baseline to 12 months.	Each participant will receive gastric antrum volume measurement both at baseline and 12 months.
Change from Baseline in Gastric Antrum Volume at 24 months.	From baseline to 24 months.	Each participant will receive gastric antrum volume measurement both at baseline and 24 months.
Change from Baseline in Gastric Emptying Time at 12 months.	From baseline to 12 months.	Each participant will receive gastric emptying time measurement both at baseline and 12 months.
Change from Baseline in Gastroparesis Cardinal Symptoms Index at 24 months.	From baseline to 24 months.	Each participant will receive gastroparesis cardinal symptoms index evaluation both at baseline and 24 months.

Trial Locations

Locations (1)

Zhongda Hospital Southeast University; 🇨🇳 Nanjing, Jiangsu, China