At a glance
ClinicalIndex Comparison RecordPhase 2Completed· 141 enrolled
Drug / intervention
Femostondrug
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.
A Prospective, Randomized, Controlled Trial Comparing 2 Different Doses of Estrogen Therapy After Hysteroscopic Adhesiolysis as an Adjuvant to Prevent Recurrence of Intrauterine Adhesions
In Brief
A Phase 2 clinical trial evaluating Femoston for Asherman Syndrome. Completed, enrolled 141 participants across 1 site.
Detailed Summary
This single-center,prospective,randomized,controlled trial is conducted to evaluate the efficacy of different doses of estrogen artificial periodic therapy after hysteroscopic adhesiolysis in patients with moderate-severe adhesion.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsAsherman Syndrome
CountriesChina
Collaborators--
Timeline
Phase 2CompletedFinished
20162017201820192020202120222023202420252026
Enrollment StartApr 2016
First PostedApr 2016
Primary CompletionAug 2016
TodayJul 2026
First PostedApr 4, 2016
Enrollment StartApr 1, 2016
Primary CompletionAug 1, 2016
TodayJul 2, 2026
Enrollment to primary: 4 monthsPosted 10.2 years ago
Interventions
Femostondrug
Femoston is a Complex Packing Estradiol Tablets and Estradiol and Dydrogesterone.