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Observational Registry for Iltamiocel Compared to Placebo for Urinary Sphincter Repair in Post-surgical Female Stress Incontinence

Study acronym: CLBT RGST
StatusEnrolling by Invitation
PhaseNot specified
Started
View on ClinicalTrials.gov ↗

Record History

  1. Re-verified, no change to tracked fieldsv5
  2. Start date changed from estimate of Apr 2025 to Apr 11, 2025v4
  3. Trial status: Not Yet Recruiting to Enrolling by Invitation
    • Start date: Mar 2025 to Apr 2025
    v3
  4. Start date: Jan 2025 to Mar 2025v2
  5. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The main purpose of this registry is to collect observational, long-term safety and effectiveness data in subjects who have received at least one dose of iltamiocel as part of the CLBT clinical study.
Trial Details
NCT Number NCT06743620
Lead Sponsor Cook MyoSite
Conditions
(from sponsor)		 Stress Urinary Incontinence
Related terms Urinary Incontinence, Stress
Enrollment 96 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov