At a glance
ClinicalIndex Comparison RecordN/ACompleted· 20 enrolled
Drug / intervention
hysteroscopic ablation of submucous uterine fibroid using diode laserdevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
In-office Hysteroscopic Laser Ablation for Symptomatic Submucous Uterine Fibroids: Impact on Size and Vascularization.
In Brief
A clinical study evaluating hysteroscopic ablation of submucous uterine fibroid using diode laser for Laser Hysteroscopic Ablation of Submucous Myoma. Completed, enrolled 20 participants across 4 sites in 3 countries.
Detailed Summary
To evaluate feasibility and efficacy of in-office hysteroscopic ablation of submucous uterine fibroid using diode laser
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesIsrael, Italy, Spain
Collaborators--
Timeline
N/ACompletedFinished
201820192020202120222023202420252026
Enrollment StartJan 2018
Primary CompletionJan 2019
Study CompletionDec 2019
First PostedNov 2022
TodayJul 2026
First PostedNov 3, 2022
Enrollment StartJan 1, 2018
Primary CompletionJan 30, 2019
Study CompletionDec 30, 2019
TodayJul 2, 2026
Enrollment to primary: 1.1 yearsPosted 3.7 years ago
Interventions
hysteroscopic ablation of submucous uterine fibroid using diode laserdevice
patients with symptomatic submucosal fibroids (heavy menstrual bleeding) were elected for hysteroscopy and laser ablation of the myoma