Table of Contents
- Trial overview
- Who can participate
- What is being measured
- Trial design and treatment groups
- Study phase and size
- What the results aim to show
Trial overview
The available trial data show one interventional study of ICEF15, called FI-3, Fidelia, with the identifier NCT04976153.[1] It is listed as authorised and is studying fecal incontinence in female and male patients.[1]
Who can participate
This study is designed for people with fecal incontinence, which means trouble controlling bowel movements.[1] The brief summary says the trial focuses on patients whose fecal incontinence is due to external anal sphincter dysfunction, caused by disruption and/or weakness of that muscle.[1]
The trial includes both female and male patients.[1] No other eligibility details are provided in the source data, so the main known target group is patients with this specific cause of fecal incontinence.[1]
What is being measured
The main outcome is the change in frequency of incontinence episodes.[1] Researchers measure this using bowel diary records, comparing the period before Visit 8, around target day 457, with the baseline period before implantation Visit 3, around target day 92.[1]
A bowel diary is a patient record of bowel movements and leakage episodes over time.[1] This helps the study team see whether the number of accidents goes down after treatment.[1]
Trial design and treatment groups
The study compares ICEF15 with placebo.[1] A placebo is a look-alike treatment used for comparison, so researchers can better judge whether changes are linked to ICEF15.[1]
Both treatments are given by intramuscular use, which means into a muscle.[1] The source data also list the study as interventional, meaning the researchers actively give a treatment and then observe the results.[1]
Study phase and size
The trial is in Phase 3.[1] Phase 3 studies are later-stage trials that usually involve more people and are meant to test how well a treatment works while continuing to watch safety.[1]
The planned enrollment is 286 participants.[1] This size suggests the researchers want enough data to make a stronger assessment of the treatment effect in the target population.[1]
What the results aim to show
The brief summary states that the main objective is the final assessment of clinical efficacy and clinical safety of ICEF15 therapy for patients with fecal incontinence caused by external anal sphincter dysfunction.[1] Clinical efficacy means how well the treatment works in the study, and clinical safety means how safely it can be used in participants.[1]
In simple terms, the trial is asking whether ICEF15 can help reduce bowel leakage and whether it can do so safely in the studied group.[1]


