Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Dysbiosis
  • Inflammatory Response
  • Pelvic Organ Prolapse
Type
Interventional
Phase
Not Applicable
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentIntervention Model Description: Participants will be randomized to the treatment arm versus standard care arm.Masking: Single (Outcomes Assessor)Masking Description: Investigators performing vaginal specimens are blinded to treatment arm.Primary Purpose: Basic Science

Participation Requirements

Age
Between 18 years and 89 years
Gender
Only males

Description

Not Provided

Not Provided

Tracking Information

NCT #
NCT04118049
Collaborators
  • University of Maryland, College Park
  • University of Connecticut
Investigators
Principal Investigator: Elisabeth Sappenfield, MD Hartford Hospital