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Clinical Trial Summary

This project will be based on three studies over a period on three years. The first study is a dose response study that includes 30 breast cancer survivors. They will receive a total of 5 laser treatments with 4-6 weeks intervals The second study is a double-blind randomized controlled trial, that includes 60 breast cancer survivors. 30 of those will receive active intervention and 30 will receive placebo laser treatment and act as controls. Based on the results of the dose response study, a treatment consists of three to five laser treatments every 3 weeks. The third and last study is a one-year follow-up on study two. The conditions are evaluated before and after each treatment by questionnaires, vaginal fluid pH values, punch biopsies and vaginal and urine microbiome. The studies is conducted at the Department of Obstetrics and Gynaecology at Randers Regional Hospital in collaboration with Department of Obstetrics and Gynaecology and Department of Oncology at Aarhus University Hospital.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Genitourinary Syndrome of Menopause
  • Syndrome

NCT number NCT06007027
Study type Interventional
Source University of Aarhus
Contact Sine Jacobsen, MD
Email sinjac@rm.dk
Status Not yet recruiting
Phase N/A
Start date March 1, 2024
Completion date July 30, 2025

See also
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