NCT06403488

Letrozole Dose Increments in PCOS Patients Resistant to Letrozole

Letrozole Dose Increments in PCOS Patients Resistant to Letrozole Ovulation Induction
Beni-Suef University·Phase 3·ClinicalTrials.gov·drugCompleted
View on ClinicalTrials.gov
Study focus
Disease/Condition
Polycystic Ovary Syndrome
Drug/Device/Intervention
Letrozole 2.5mg
Study type
Interventional
Intervention type
drug
Sponsor & location
Primary sponsor
Beni-Suef University
Location
Banī Suwayf,Banī Suwayf, Egypt
Timeline & enrollment
Phase
Phase 3
Start date
Oct 01, 2023
End date
Jan 30, 2024
Enrollment
102 participants
Primary outcome

ovulation rate,endometrial thickness

Summary

Objectives: To study the effect of Letrozole dose increments on ovulation rate and
 endometrial thickness as a primary outcomes in patients with polycystic ovary syndrome who
 previously resistant to letrazole conventional dose, and chemical and clinical pregnancy
 considered as secondary outcomes.

ICD-10 classifications
Polycystic ovarian syndromeOvarian dysfunction, unspecifiedOvarian dysfunctionOther ovarian dysfunctionNeoplasm of uncertain or unknown behaviour: Ovary
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT06403488
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT06403488 through Pure Global AI's free database. This Phase 3 trial is sponsored by Beni-Suef University and is currently Completed. The study focuses on Polycystic Ovary Syndrome. Target enrollment is 102 participants.

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