About this trial
To evaluate the safety and efficacy of endoscopic full thickness biopsy for the diagnostic purpose of chronic intestinal pseudo-obstruction.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Patients with chronic pseudo intestinal obstruction or suspected chronic pseudo intestinal obstruction
Patients who are 18 years of age or older at the time of obtaining consent
Gender: Any
Disqualifiers
Patients for whom it is difficult to perform endoscopy
Patients who cannot obtain consent
Patients with serious renal, hepatic, or cardiac disease
Patients who are participating in other clinical research, except for observational research.
Trial design
Single group
Treatments tested in this trial
Over the scope clip
Deviceover the scope clip group
Treatment groups
Trial outcomes
Primary outcomes
Percentage of total perforations (intraoperative and delayed perforations)
Percentage of total perforations (intraoperative and delayed perforations)
Secondary outcomes
Intraoperative perforation rate
Intraoperative perforation rate
Rate of delayed perforation
Rate of delayed perforation
Intraoperative complications
Intraoperative complications
Intraoperative death rate
Intraoperative death rate
Sponsors and contacts
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This trial is not recruiting at the moment. You can still explore other options: