Perianal Operating Scope Feasibliity

Withdrawn before enrolling · Not applicable

Conditions studied: Transanal Endoscopic Surgery

In brief

This protocol will test a new prototype of a peri-anal access device, with increased flexible length and a captured operative field, for feasibility in patients immediately prior to their scheduled peri-anal procedure.

Key facts

Study ID

NCT02807792

Run by

University of Minnesota

People needed

0

Starts

2017-07-01

Expected to finish

2018-07-01

Last updated by the study team

2017-04-27

Who can join

Age: 18 and older, up to 80. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Age range 18 to 80
• In good health status
• Patients scheduled for a transanal procedure other than for anal lesions, e.g., hemorrhoids, fissures, abscesses

You may not qualify if…

• Patients with physical characteristics that distort the rectal sigmoid anatomy, e.g., spinal lesions.
• Patients considerable unsuitable for inclusion in the study by their colorectal surgeon.
• Patients considered too frail or ill by their physician to undergo a 5-10 minute prolongation of their procedure.
• Patients with known rectosigmoid infections.
• Patients with known rectosigmoid wall fragility.
• Patients with known rectosigmoid perforations.

Where it is running

• University of Minnesota — Minneapolis, Minnesota, United States

Full record on ClinicalTrials.gov

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