Women's Satisfaction and Adherence to Vulvovaginal Atrophy Treatments

NCT04607707 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 831

Last updated 2021-06-21

No results posted yet for this study

Summary

The primary objective of this study is to describe and assess participants' satisfaction with current vulvovaginal atrophy (VVA) treatment.

Conditions

  • Vulvovaginal Atrophy

Sponsors & Collaborators

  • Shionogi

    lead INDUSTRY

Principal Investigators

  • Shionogi Clinical Trials Administrator Clinical Support Help Line · Shionogi

Eligibility

Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-07-07
Primary Completion
2021-04-30
Completion
2021-04-30

Countries

  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04607707 on ClinicalTrials.gov