Clin2
NCT05648253Possibly a fitRecruiting

Hyivy device after pelvic radiation for vaginal health

Vaginal StenosisRadiation TherapyCancerPelvic PainPelvic Cancer

Part of Cancer, Pain clinical trials.

This study checks whether a special vaginal device (Hyivy) is safe and workable after pelvic radiation for certain cancers. You may be asked to use it for 12 weeks to help with vaginal changes after treatment, and you would visit the study team regularly.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
12 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • Be 18 years or older and able to follow the study plan and consent
  • Have completed pelvic radiation for endometrial, cervical, anal, or rectal cancer (no chemotherapy at the same time)
  • Be post-menopausal for at least 1 year, or be surgically sterile, or use reliable birth control if you could become pregnant
  • Plan to use only the study’s dilators/device (not other vaginal dilators) for 12 weeks
  • Be able to insert the device yourself and charge the device as instructed
  • Have no active vaginal/pelvic infection, open sores, or allergy to the device materials

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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