Recruitment

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