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Safety and Efficacy of Underwater Endoscopic Mucosal Resection for Type I Gastric Neuroendocrine Tumors Measuring 5-9 mm

Safety and Efficacy of Underwater Endoscopic Mucosal Resection for Type I Gastric Neuroendocrine Tumors Measuring 5-9 mm: A Prospective Single-Centre Cohort Study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07728292
Acronym
POEM
Enrollment
60
Registered
2026-07-27
Start date
2026-07-17
Completion date
2026-12-30
Last updated
2026-07-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stomach Neuroendocrine Neoplasm

Brief summary

Study objectives: Primary objective: 1.To determine the histologic R0 resection rate of UEMR for type I gastric NETs measuring 5-9 mm. Secondary objectives: To evaluate: 1. En bloc resection rate 2. Immediate and delayed adverse events 3. Procedure time 4. Histologic quality of resection (deep and lateral margins) 5. Residual disease at resection scar on surveillance endoscopy oMetachronous gastric NETs during follow-up

Detailed description

Study design This is a prospective, single-centre, single-arm cohort study evaluating UEMR for type I gastric NETs. Outcomes will be assessed at the lesion level, with statistical methods accounting for clustering of multiple lesions within individual patients. Study population Inclusion criteria Patient-level 1. Age ≥18 years 2. Fit for endoscopic therapy and sedation 3. Written informed consent Lesion-level 3.Endoscopically visible gastric neuroendocrine tumor 4.Size 5-9 mm (endoscopic estimation) 5.Clinical and/or histologic features consistent with type I gastric NET 6.No endoscopic features suggestive of deep invasion 7.Technically amenable to snare resection Exclusion criteria Lesion-level 1. Lesions \<5 mm (managed with surveillance in routine practice) 2. Lesions ≥10 mm 3. Type II or type III gastric NET 4. Evidence of muscularis propria invasion on EUS 5. Distant metastasis or nodal disease on DOTANOC PET-CT 6. Prior attempted resection at the same site with significant fibrosis 7. Non-lifting lesion due to scarring Patient-level 1. Uncorrectable coagulopathy 2. Inability to manage antithrombotic therapy as per guidelines 3. Pregnancy 4. Inability to provide informed consent Pre-procedure evaluation 1. Detailed clinical assessment and laboratory work-up as per institutional protocol 2. Endoscopic documentation of: 3. Lesion size, location, morphology 4. Number of lesions 5. Background mucosal atrophy 6. EUS performed for lesions ≥8 mm, atypical morphology, or suspected deeper invasion 7. DOTANOC PET-CT performed where clinically indicated to exclude metastatic disease Intervention: Underwater EMR technique 1. Standard diagnostic gastroscope 2. Minimal insufflation followed by complete deflation of the gastric lumen 3. Lumen filled with normal saline to achieve complete submersion of the lesion 4. Optional marking for flat or ill-defined lesions 5. Snare capture with a 1-2 mm margin under water 6. Resection using standardized electrosurgical settings 7. Defect management (clips or coagulation) at endoscopist discretion 8. Retrieval of intact specimen 9. Specimen orientation and pinning on cork for histopathologic assessment Histopathologic assessment: All specimens will be evaluated by experienced gastrointestinal pathologists. Reported parameters: 1. Tumor size 2. Tumor grade and Ki-67 index 3. Depth of invasion 4. Lateral and vertical margins 5. Lymphovascular invasion 6. Resection status classified as: 7. R0: negative lateral and vertical margins 8. R1: microscopic margin positivity 9. Rx: indeterminate margins Outcome measures Primary outcome 1. R0 resection rate per lesion Secondary outcomes 2. En bloc resection rate 3. Immediate bleeding (requiring endoscopic hemostasis) 4. Delayed bleeding (within 14 days requiring medical attention) 5. Perforation 6. Procedure time (scope insertion to removal) 7. Residual disease at scar on surveillance endoscopy (3-6 months) 8. Metachronous lesions during follow-up Follow-up protocol 1. Clinical follow-up at 24-72 hours and at 14 days 2. Surveillance endoscopy at 3-6 months post-resection 3. Further surveillance as per institutional protocol for type I gastric NETs

Interventions

PROCEDUREEndoscopic mucosal resection under water

* Standard diagnostic gastroscope * Minimal insufflation followed by complete deflation of the gastric lumen * Lumen filled with normal saline to achieve complete submersion of the lesion * Optional marking for flat or ill-defined lesions * Snare capture with a 1-2 mm margin under water * Resection using standardized electrosurgical settings * Defect management (clips or coagulation) at endoscopist discretion * Retrieval of intact specimen * Specimen orientation and pinning on cork for histopathologic assessment

Sponsors

Asian Institute of Gastroenterology, India
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

Patient-level * Age ≥18 years * Fit for endoscopic therapy and sedation * Written informed consent

Exclusion criteria

Lesion-level * Endoscopically visible gastric neuroendocrine tumor * Size 5-9 mm (endoscopic estimation) * Clinical and/or histologic features consistent with type I gastric NET * No endoscopic features suggestive of deep invasion * Technically amenable to snare resection

Design outcomes

Primary

MeasureTime frameDescription
• To determine the histologic R0 resection rate of UEMR for type I gastric NETs measuring 5-9 mm.3 monthsNo recurrence after 3 months of procedure

Secondary

MeasureTime frameDescription
Immediate and delayed adverse events24 hoursTo check any possible adverse events post procedure
Procedure time30 minutesTo calculate the exact time of procedure
Histologic quality of resection (deep and lateral margins)5 daysTo check the depth of invasion of the tumour

Countries

India

Contacts

CONTACTRajesh Mr Goud, M.Pharmacy
rajeshgoud761@gmail.com04023378888
CONTACTShashavali Dr Maniyar, MD
shashimaniyar@gmail.com04023378888
PRINCIPAL_INVESTIGATORZaheer Dr Nabi, MD

AIG HOSPITALS

STUDY_CHAIRMohan Dr Ramchandani, MD

AIG HOSPITALS

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 28, 2026