Gastroparesis Clinical Trial
Official title:
Endoscopic Clips Versus Overstich Suturing System Device for Closure of Mucosotomy After Per-oral Endoscopic Pyloromyotomy (G-POEM)
Verified date | January 2021 |
Source | Institute for Clinical and Experimental Medicine |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Gastric per-oral endoscopic pyloromyotomy (G-POEM) has been assessed as new modality for treatment of refractory gastroparesis. G-POEM is promising method, which is still under investigation as its safety and efficacy has not been established yet. The ideal closure technique in patients undergoing G-POEM needs to be established. Several techniques may be used for endoscopic mucosal closure: endoscopic clips, OTSC (over the scope clips), endo-loop based methods (KING closure) or endoscopic suture. The aim of this prospective, open-label study is to compare efficacy and safety of two methods for incision closure in patients who undergo G-POEM: endoscopic clips vs. endoscopic suturing system (OverStitch).
Status | Completed |
Enrollment | 40 |
Est. completion date | January 26, 2021 |
Est. primary completion date | December 1, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 90 Years |
Eligibility | Inclusion Criteria: 1. Refractory (> 6 months) and severe (based on a validated total Gastroparesis Cardinal Symptom Index) gastroparesis, with confirmed gastric emptying based on a gastric emptying study: standardized protocol of scintigraphy in all patients (performed less than 6 months prior to enrolment). The total GSCI (Gastroparesis Cardinal Symptom Index) score must be >2.0 - Abnormal gastric emptying is defined as retention of Tc-99 m >60% at 2 h and/or =10% of residual activity at 4 h on a standardized sulphur colloid solid-phase gastric emptying study. - Abnormal gastric emptying breath test based on a solid normal range determination for the test used (e.g. T1/2 > 109 min) 2. Severe refractory disease is defined as GCSI >2.0 and failure or recurrence in patients who received available optimal pharmacological therapies. 3. Persons 18 years or older at the time of signing the informed consent 4. Signed informed consent Exclusion Criteria: 1. No previous attempt with at least one prokinetic drug 2. No previous attempt to withdraw anticholinergic agents and glucagon like peptide -1 (GLP-1) and amylin analogues in patients treated with these substances 3. Active treatment with opioids or a history of treatment with opioids within 12 months before enrolment 4. Previous gastric surgery (Billroth I or Billroth II) 5. Known eosinophilic gastroenteritis 6. Organic pyloric (or intestinal) obstruction (fibrotic stricture, etc.) 7. Sever coagulopathy 8. Oesophageal or gastric varices and /or portal gastropathy 9. Advanced liver cirrhosis (Child B or Child C) 10. Active peptic ulcer disease 11. Pregnancy or puerperium 12. Malignant or pre-malignant gastric diseases (dysplasia, gastric cancer, GIST): patients with a history of such disease after its cure are eligible for enrolment 13. Any other condition, which in the opinion of the investigator would interfere with study requirements 14. Uncontrolled diabetes mellitus 15. Diagnosis of rumination syndrome or "eating" disorder (mental anorexia, bulimia nervosa) 16. Inability to obtain informed consent |
Country | Name | City | State |
---|---|---|---|
Czechia | Institute for Clinical and Experimental Medicine | Prague 4 | Prague |
Lead Sponsor | Collaborator |
---|---|
Institute for Clinical and Experimental Medicine |
Czechia,
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Dacha S, Mekaroonkamol P, Li L, Shahnavaz N, Sakaria S, Keilin S, Willingham F, Christie J, Cai Q. Outcomes and quality-of-life assessment after gastric per-oral endoscopic pyloromyotomy (with video). Gastrointest Endosc. 2017 Aug;86(2):282-289. doi: 10.1 — View Citation
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Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Proportion of subjects with successful and safe incision closure. | Definition of successful closure: endoscopically completely closed incision, no need to use another "rescue" closure method, no leak on post-operative day 1, no leak related complications, no readmission due to closure dehiscence, no need for surgery due to closure. | 3 months | |
Secondary | Easiness of the closure | Handling with endoclips or OverStitch will be evaluated by means of a questionnaire where ease of use was scored on a VAS (visual analogue scale), 0 = impossible, 10 = very easy) by both, endoscopist as well as an endoscopy nurse assisting with the closure procedure. | 3 months | |
Secondary | Closure time of mucosotomy | The duration of endoscopic closure, reported by the endoscopist performing the procedure | 1 day | |
Secondary | Cost | To evaluate the economics and cost-effectiveness of treating gastroparesis | 3 months | |
Secondary | Healing quality | Assessing gastric scar after gastric per-oral pyloromyotomy: based on a visual examination, the healing process could include three stages, namely stage A (active stage): means no tissue reparation features, stage H (healing stage): early morphological reparation features, and stage S (scar stage): completed repair process, that could by described as S1 (red) or S2 (white). Width and length of scar will be measures as well. | 3 months | |
Secondary | Readmission within 30 days | A readmission for an endoscopic or surgery intervention to address a complication resulting from care during the initial admission. | 30 days | |
Secondary | Mortality at 3 months | Incidence of fatal complications related to procedure | 3 months |
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