CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 8 enrolled
Drug / intervention
Not specified
Likely dose
Not stated in record
Key inclusion· 6
  • ✓Age 18–45 years at prescreening
  • ✓Reported vaginal sex with a man in the past month
  • ✓Not pregnant and no intention to become pregnant during study
  • ✓Negative or unknown HIV status
Key exclusion· 8
  • ✕Pregnant or intend to become pregnant during study
  • ✕Currently breastfeeding
  • ✕Vaginal delivery or reproductive surgical procedure in past 30 days
  • ✕HIV-positive status

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02057419
NCT02057419N/ACompleted
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K24: Advancing Reproductive Health: Women's Input on Sexual Health (Project WISH)

The Miriam Hospital·observational·Posted Feb 7, 2014·Updated Oct 24, 2025

In Brief

An observational study for Intravaginal Ring Use. Completed, enrolled 8 participants across 1 site.

Detailed Summary

The purpose of this study is to answer the following question: How do user sensory perceptions and experiences (USPEs) for IVRS differ between initial and continued use and how can this knowledge help product developers better understand how to design new IVR products and develop behavioral (or point-of-care) interventions to optimize use?

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsIntravaginal Ring Use
CountriesUnited States
CollaboratorsEunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

Timeline

N/ACompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedFeb 7, 2014
Enrollment StartApr 14, 2014
Primary CompletionJun 24, 2016
Study CompletionMar 31, 2018
TodayJul 2, 2026
Enrollment to primary: 2.2 yearsPosted 12.4 years ago