Safety and Feasibility Evaluation of ALVIV Laser Based Treatment for Fecal Incontinence

Recruiting now · Not applicable

Conditions studied: Fecal Incontinence (FI)

In brief

The purpose if this interventional First in Human study is to assess the Safety and Performance of the ALVIV System laser based treatment in patients diagnosed with Fecal Incontinence. Eligible patients will go through screening assessments, followed by a series of 4-6 treatments with 3 weeks apart. Last follow up visit to the study will occur 3 weeks after last treatment day. Participants will be asked to maintain a diary of their fecal incontinence episodes, and complete quality of life and satisfaction questionnaires throughout the study.

Key facts

Study ID
NCT07436676
Run by
Alviv Ltd.
People needed
12
Starts
2024-04-03
Expected to finish
2026-03-01
Last updated by the study team
2026-02-27

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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