Study of Oxytocin to Treat Vaginal Atrophy in Postmenopausal Women
Sponsored by PepTonic Medical AB
About this trial
Last updated 14 years ago
Study ID
Status
Type
Phase
Placebo
Accepting
Not accepting
Trial Timing
Ended 14 years ago
What is this trial about?
What are the participation requirements?
Inclusion Criteria
- Signed Informed Consent
- at least 40 years of age
- naturally postmenopausal women, completely without menstrual bleedings for at least four years prior to screening.
- FSH plasma levels at least 40 IU/L and 17β-estradiol levels less than 70pmol/L
- Vaginal pH more than 5.0
- BMI at most 29 kg/m2
- Vaginal atrophy verified by cytological assessment of the vaginal mucosal epithelium. Vaginal atrophy is defined as at most 5% of superficial cells.
Exclusion Criteria
- Usage of any sex steroids including phytoestrogens, hormonal intra-uterine device or herbal medicinal products with known estrogenic effects within 3 months prior to screening.
- Usage of any lubricant for intra-vaginal administration at inclusion
- Any condition that is a contraindication to treatment with sex steroids
- Vaginal bleeding of unknown origin
- Any untreated urogenital infection within 7 days prior to inclusion
- Any prior or concurrent malignant disease or endometrial hyperplasia
- Cervical cytology at least CIN 1 assessed during screening
- Clinically significant medical history (excluding medically well-controlled hypertension and hypercholesterolemia), findings from physical examinations, vital signs, cytology, histology or laboratory analyses that may interfere with the study objectives or compromise the safety of the subject as judged by the Investigator.
- Systolic Blood Pressure at least 140 mmHg or Diastolic Blood Pressure at least 90 mmHg at screening
- Participation in any other interventional clinical trial within 3 months prior to screening
- Known or suspected drug or alcohol abuse, within 12 months prior to screening
- Concurrent and diagnosed nephrologic or hepatic disorder
- Diagnosed with HIV, Hepatitis B or C
- Known or suspected allergy to any ingredient of the study product
- Incapacity to perform study procedures, as judged by the Investigator