Safety and Efficacy of Endoscopic Full Thickness Biopsy in Patients With Chronic Intestinal Pseudo-obstruction

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorInternational University of Health and Welfare

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 volunteers

Qualifiers

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

Design model

Single group

Treatments tested in this trial

  • Over the scope clip

    Device

    over the scope clip group

Treatment groups

20 Participants
are divided into 1 treatment group
Group A: Over the scope clipExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Percentage of total perforations (intraoperative and delayed perforations)

Percentage of total perforations (intraoperative and delayed perforations)

Time frame
Immediately after the intervention

Secondary outcomes

1

Intraoperative perforation rate

Intraoperative perforation rate

Time frame
Under procedure
2

Rate of delayed perforation

Rate of delayed perforation

Time frame
Periprocedural
3

Intraoperative complications

Intraoperative complications

Time frame
Under procedure
4

Intraoperative death rate

Intraoperative death rate

Time frame
Under procedure

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: