At a glance
ClinicalIndex Comparison RecordN/ACompleted· 20 enrolled
Drug / intervention
s.c 25 mg estradiol pelletdrug
Likely dose
s.c 25 mg estradiol pelletfrom 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.
Pharmacokinetic Aspects of 25-mg Estradiol Pellet in Climacteric Women Comprehensive Longitudinal Assessment of Release With Estradiol Pellet Analysis (CLARA Study)
In Brief
A clinical study evaluating s.c 25 mg estradiol pellet for Climacteric Syndrome and 2 related conditions. Completed, enrolled 20 participants across 1 site.
Detailed Summary
A single center, prospective, open-label clinical study will be conducted, to monitor serum concentration and pharmacokinetic profile after subcutaneous implantation of a 25mg-estradiol bioabsorbable implant in postmenopausal women.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsClimacteric Syndrome, Menopause, Hypoestrogenism
CountriesBrazil
CollaboratorsBiòs Farmacêutica
Timeline
N/ACompletedFinished
202420252026
First PostedNov 2023
Enrollment StartDec 2023
Primary CompletionOct 2024
Study CompletionJul 2025
TodayJul 2026
First PostedNov 18, 2023
Enrollment StartDec 13, 2023
Primary CompletionOct 9, 2024
Study CompletionJul 30, 2025
TodayJul 2, 2026
Enrollment to primary: 10 monthsPosted 2.6 years ago
Interventions
s.c 25 mg estradiol pelletdrug
Subcutaneous insertion of 25 mg estradiol pellet.