Intravaginal Prasterone (DHEA) Against Vulvovaginal Atrophy Associated With Menopause

Phase 3CompletedNCT02013544

EndoCeutics Inc.558 enrolled

Overview

The purpose of this study is to confirm the efficacy of intravaginal prasterone (DHEA) on symptoms of vulvovaginal atrophy due to menopause and to collect further data on subjects exposed to intravaginal DHEA in order to meet the ICH E1 guideline requirements.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

QUADRUPLE

Enrollment

558

Conditions

Vaginal Atrophy

Interventions

PlaceboDRUG

Prasterone (DHEA)DRUG

Eligibility

Sex: FEMALEMin age: 40 YearsMax age: 80 Years

Medical Language ↔ Plain English

Inclusion Criteria: Main criteria: * Postmenopausal women (hysterectomized or not) * Women between 40 and 80 years of age * Women having ≤5% of superficial cells on vaginal smear at baseline * Women having a vaginal pH above 5 at baseline * Women who have self-identified moderate or severe symptom(s) of vaginal atrophy * Willing to participate in the study and sign an informed consent Exclusion Criteria: Main criteria: * Previous enrollment in EndoCeutics studies performed with intravaginal DHEA * Previous diagnosis of cancer, except skin cancer (non melanoma) * Clinically significant metabolic or endocrine disease (including diabetes mellitus) not controlled by medication * The administration of any investigational drug within 30 days of screening visit * Clinically significant abnormal serum biochemistry, urinalysis or hematology

Locations (38)

Outcomes

Primary Outcomes

Change From Baseline to Week 12 in Percentage of Superficial Cells in the Maturation Index of the Vaginal Smear

The percentage of superficial cells was determined from the vaginal smears collected during the study. A 100-cell count was performed by a central laboratory to classify cells as parabasal (P) (including basal), intermediate (I), and superficial (S) squamous cell types. Data obtained at Baseline and Week 12 as well as the change from Baseline to Week 12 are presented.

Time frame: Baseline and Week 12

Change From Baseline to Week 12 in Percentage of Parabasal Cells in the Maturation Index of the Vaginal Smear

The percentage of parabasal cells was determined from the vaginal smears collected during the study. A 100-cell count was performed by a central laboratory to classify cells as parabasal (P) (including basal), intermediate (I), and superficial (S) squamous cell types. Data obtained at Baseline and Week 12 as well as the change from Baseline to Week 12 are presented.

Time frame: Baseline and Week 12

Change From Baseline to Week 12 in Vaginal pH

A pH strip fixed on an Ayre spatula (or equivalent) was applied directly to the lateral wall of the vagina. The change in color of the pH indicator strip was compared to the color chart for pH evaluation. The corresponding pH value (with one decimal) was recorded. Data obtained at Baseline and Week 12 as well as the change from Baseline to Week 12 are presented.

Time frame: Baseline and Week 12

Change From Baseline to Week 12 in Severity of the Most Bothersome Symptom of Dyspareunia

The severity of dyspareunia was evaluated by a questionnaire filled out by women. The severity of dyspareunia recorded as none, mild, moderate or severe was analyzed using the score values of 0, 1, 2 or 3, respectively. Data obtained at Baseline and Week 12 as well as the change from Baseline to Week 12 are presented.

Time frame: Baseline and Week 12

Secondary Outcomes

Data from ClinicalTrials.gov

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EndoCeutics site # 39

Montgomery, Alabama, United States

EndoCeutics site # 14

Tucson, Arizona, United States

EndoCeutics site # 21

Sacramento, California, United States

EndoCeutics site # 83

San Diego, California, United States

EndoCeutics site # 30

San Diego, California, United States

EndoCeutics site # 36

Denver, Colorado, United States

EndoCeutics site # 52

Denver, Colorado, United States

EndoCeutics site # 45

Boynton Beach, Florida, United States

EndoCeutics site # 60

Lake Worth, Florida, United States

EndoCeutics site # 54

North Miami, Florida, United States

...and 28 more locations

Change From Baseline to Week 12 in Severity of Vaginal Dryness

The severity of vaginal dryness was evaluated by a questionnaire filled out by women. The severity of vaginal dryness recorded as none, mild, moderate or severe was analyzed using the score values of 0, 1, 2 or 3, respectively. Data obtained at Baseline and Week 12 as well as the change from Baseline to Week 12 are presented.

Time frame: Baseline and Week 12

Change From Baseline to Week 12 in Severity of Vaginal Atrophy as Evaluated From Vaginal Secretions

To evaluate the aspect of the mucosa and the local tolerance to prasterone ovules, the vaginal secretions (one of the four main signs of vaginal atrophy) evaluated by the physician/gynecologist as corresponding to none, mild, moderate, or severe atrophy were analyzed using the score values of 1, 2, 3 and 4, respectively. Data obtained at Baseline and Week 12 as well as the change from Baseline to Week 12 are presented.

Time frame: Baseline and Week 12

Change From Baseline to Week 12 in Severity of Vaginal Atrophy as Evaluated From Vaginal Epithelial Integrity

To evaluate the aspect of the mucosa and the local tolerance to prasterone ovules, the vaginal epithelial integrity (one of the four main signs of vaginal atrophy) evaluated by the physician/gynecologist as corresponding to none, mild, moderate, or severe atrophy was analyzed using the score values of 1, 2, 3 and 4, respectively. Data obtained at Baseline and Week 12 as well as the change from Baseline to Week 12 are presented.

Time frame: Baseline and Week 12

Change From Baseline to Week 12 in Severity of Vaginal Atrophy as Evaluated From Vaginal Epithelial Surface Thickness

To evaluate the aspect of the mucosa and the local tolerance to prasterone ovules, the vaginal epithelial surface thickness (one of the four main signs of vaginal atrophy) evaluated by the physician/gynecologist as corresponding to none, mild, moderate, or severe atrophy was analyzed using the score values of 1, 2, 3 and 4, respectively. Data obtained at Baseline and Week 12 as well as the change from Baseline to Week 12 are presented.

Time frame: Baseline and Week 12

Change From Baseline to Week 12 in Severity of Vaginal Atrophy as Evaluated From Vaginal Color

To evaluate the aspect of the mucosa and the local tolerance to prasterone ovules, the vaginal color (one of the four main signs of vaginal atrophy) evaluated by the physician/gynecologist as corresponding to none, mild, moderate, or severe atrophy was analyzed using the score values of 1, 2, 3 and 4, respectively. Data obtained at Baseline and Week 12 as well as the change from Baseline to Week 12 are presented.

Time frame: Baseline and Week 12