Impact of Different Doses and Routes of Exogenous Progesterone Administration on Endometrial Receptivity Parameters
Last updated on July 2021Recruitment
- Recruitment Status
- Not yet recruiting
- Estimated Enrollment
- Same as current
Summary
- Conditions
- ENDOMETRIAL RECEPTIVITY
- Infertility Female
- Type
- Interventional
- Phase
- Phase 4
- Design
- Allocation: RandomizedIntervention Model: Parallel AssignmentIntervention Model Description: Exploratory, unicentric, with blind evaluators, randomized to six parallel arms in ratio 1:1:1:1:1:1 clinical trial conducted in healthy volunteers under an artificial endometrial preparation cycle and luteal phase support with exogenous progesterone administered by different doses and routes or natural menstrual cycles.Masking: Single (Investigator)Masking Description: Patients will be evaluated by blinded gynecologist in order to prevent the application of personal criteria and protect the consistence of the study.Primary Purpose: Treatment
Participation Requirements
- Age
- Between 18 years and 35 years
- Gender
- Only males
Description
Not Provided
Not Provided
Tracking Information
- NCT #
- NCT04499131
- Collaborators
- Not Provided
- Investigators
- Not Provided