At a glance
ClinicalIndex Comparison RecordN/ACompleted· 45 enrolled
Drug / intervention
Apollo ESG with ERBE HAPC +1 moredevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Hybrid Argon Plasma Coagulation and Endoscopic Sleeve Gastroplasty Trial (HAPCET): A Single-center Randomized Controlled Trial
In Brief
A clinical study evaluating Apollo ESG with ERBE HAPC and Apollo ESG for Obesity. Completed, enrolled 45 participants across 1 site.
Detailed Summary
This study is being done to evaluate the safety and effectiveness of combined Hybrid Argon Plasma Coagulation (HAPC) and Endoscopic Sleeve Gastroplasty (ESG) for weight loss and improvement in obesity-related co-morbidities compared to ESG alone in participants with a BMI ≥ 30 and ≤40 kg/m² who have failed to achieve and maintain weight loss with a non-surgical program.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsObesity
CountriesUnited States
CollaboratorsErbe Elektromedizin GmbH
Timeline
N/ACompletedFinished
2023202420252026
First PostedSep 2022
Enrollment StartNov 2022
Primary CompletionAug 2024
Study CompletionJan 2025
TodayJul 2026
First PostedSep 29, 2022
Enrollment StartNov 18, 2022
Primary CompletionAug 2, 2024
Study CompletionJan 17, 2025
TodayJul 2, 2026
Enrollment to primary: 1.7 yearsPosted 3.8 years ago
Interventions
Apollo ESG with ERBE HAPCdevice
Utilizing two approved devices in combination to assess durability of suturing.
Apollo ESGdevice
Using only Apollo ESG as approved per label.