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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01400776
Other study ID # PR-04409.3
Secondary ID
Status Completed
Phase Phase 3
First received
Last updated
Start date June 29, 2011
Est. completion date February 27, 2012

Study information

Verified date September 2021
Source Warner Chilcott
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Study if WC3011 is effective and safe in the treatment of postmenopausal vaginal dryness due to vulvovaginal atrophy.


Recruitment information / eligibility

Status Completed
Enrollment 722
Est. completion date February 27, 2012
Est. primary completion date February 27, 2012
Accepts healthy volunteers No
Gender Female
Age group 35 Years and older
Eligibility Inclusion Criteria: - Postmenopausal females =35 years with either or both ovaries removed or naturally menopausal with moderate to severe vaginal dryness Exclusion Criteria: - Hypersensitivity to estrogen and/or progestin therapy - Known or suspected premalignant or malignant disease (except successfully treated skin cancers) - Manifestation of or treatment for significant cardiovascular disease, congestive heart failure, stroke or ischemic attacks - Insulin-dependent diabetes mellitus - Increased frequency or severity of headaches while on hormone or estrogen therapy - Drug or alcohol addiction within last 2 years - Participation in a clinical trial within 30 days - Smoking = 15 cigarettes daily - Uncontrolled hypertension - systolic blood pressure (BP) = 160 mmHg or diastolic BP = 95 mmHg

Study Design


Related Conditions & MeSH terms

  • Atrophy
  • Postmenopausal Vulvovaginal Atrophy

Intervention

Drug:
WC3011 Estradiol Vaginal Cream
WC3011 estradiol vaginal cream administered once daily for 2 weeks followed by 2X/week or 3X/week for 10 weeks, total treatment duration 12 weeks
Vehicle
Vehicle administered once daily for 2 weeks followed by 2X/week or 3X/week for 10 weeks, total treatment duration 12 weeks.

Locations

Country Name City State
United States Radiant Research-Atlanta Atlanta Georgia
United States Kentucky Pediatric Research, Inc. Bardstown Kentucky
United States Fellows Research Alliance, Inc. Bluffton South Carolina
United States Visions Clinical Research Boynton Beach Florida
United States Ridgeview Research Two Twelve Medical Center Chaska Minnesota
United States Radiant Research-Chicago Chicago Illinois
United States Women's Medical Research Group, LLC Clearwater Florida
United States Rapid Medical Research, Inc. Cleveland Ohio
United States SC Clinical Research Center, LLC Columbia South Carolina
United States The Columbus Center for Women's Health Research Columbus Ohio
United States Practice Research Organization, Inc. Dallas Texas
United States Radiant Research-Dallas Dallas Texas
United States Research Across America RHD Professional Plaza 4 Dallas Texas
United States Soapstone Center for Clinical Research Decatur Georgia
United States HWC - Women's Research Center Englewood Ohio
United States Clinical Trials of America, Inc. Eugene Oregon
United States The South Bend Clinic, LLP Granger Indiana
United States Hawthorne Medical Research, Inc. Greensboro North Carolina
United States Advances in Health, Inc. Houston Texas
United States Medical Affiliated Research Center, Inc. Huntsville Alabama
United States Jacksonville Center for Clinical Research Jacksonville Florida
United States The Clinical Trial Center, LLC Jenkintown Pennsylvania
United States Beyer Research Kalamazoo Michigan
United States Physicians' Research Options LLC Lakewood Colorado
United States Affiliated Clinical Research Las Vegas Nevada
United States Lawrence OB-GYN Associates, P.C. Lawrenceville New Jersey
United States Bluegrass Clinical Research, Inc. Louisville Kentucky
United States York Clinical Consulting Marrero Louisiana
United States Advanced Clinical Research Medford Oregon
United States Miami Research Associates Miami Florida
United States New Age Medical Research Corp Miami Florida
United States Mobile OB-GYN, PC Mobile Alabama
United States Phoenix OB-GYN Assoc., LLC Moorestown New Jersey
United States Eastern Carolina Women's Center New Bern North Carolina
United States Costal Connecticut Resarch, LLC New London Connecticut
United States Women Under Study New Orleans Louisiana
United States Eastern Virginia Medical School Norfolk Virginia
United States Ormond Medical Arts Pharmaceutical Research Center Ormond Beach Florida
United States Radiant Research - Overland Park Overland Park Kansas
United States OB-GYN Specialists of the Palm Palm Beach Gardens Florida
United States Philadelphia Clinical Research, LLC Philadelphia Pennsylvania
United States Precision Trials, LLC Phoenix Arizona
United States Women's Health Research Phoenix Arizona
United States Radiant Research-St. Petersburg Pinellas Park Florida
United States Clinical Trials Research Services, LLC Pittsburgh Pennsylvania
United States The Center for Women's Health and Wellness, LLC Plainsboro New Jersey
United States Wake Research Associates, LLC Raleigh North Carolina
United States Virginia Women's Center Richmond Virginia
United States Atlanta North Gynecology, PC Roswell Georgia
United States J. Lewis Research - Foothill Family Clinic South Salt Lake City Utah
United States J. Lewis Research-foothill Family Clinic Salt Lake City Utah
United States Radiant Research-San Antonio San Antonio Texas
United States Genesis Center for Clinical Research San Diego California
United States Medical Center for Clinical Research San Diego California
United States Women's Healthcare Inc. San Diego California
United States Physicians' Research Options LLC Sandy Utah
United States Fellows Research Alliance, Inc. Savannah Georgia
United States Radiant Research-Scottsdale Scottsdale Arizona
United States Seattle Women's: Health, Research Gynecology Seattle Washington
United States North Spokane Women's Clinic Spokane Washington
United States Springfield Clinical, LLP Springfield Illinois
United States Radiant Research-Tucson Tucson Arizona
United States Visions Clinical Research-tucson Tucson Arizona
United States Omega Medical Research Warwick Rhode Island
United States Center for Reproductive Medicine Webster Texas
United States Comprehensive Clinical Trials, LLC West Palm Beach Florida
United States Susan L. Floyd, MD, PC Wexford Pennsylvania
United States Heartland Research Associates Wichita Kansas
United States Hawthorne Medical Research, Inc. Winston-Salem North Carolina
United States Lyndhurst Clinical Research Winston-Salem North Carolina

Sponsors (1)

Lead Sponsor Collaborator
Warner Chilcott

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change From Baseline in Participant's Self-Assessment of Severity of Vaginal Dryness to Week 12/Final Visit The severity of vaginal dryness was assessed and recorded on a questionnaire by the participants using the following 4 point scale where, 0=None (The symptom is not present), 1=Mild (The symptom is present but may be intermittent; does not interfere with participants activities or lifestyle), 2=Moderate (The symptom is present. Participant is usually aware of the symptom, but activities and lifestyle are only occasionally affected), and 3=Severe (The symptom is present. Participant is usually aware and bothered by the symptom and have modified participant's activities and/or lifestyle due to the symptom. The negative change from Baseline indicates improvement. Week 12/Final Visit is defined as the last available postbaseline assessment up to Week 12. Baseline (Day 0) to Week 12/Final Visit
Primary Change From Baseline in Vaginal pH to Week 12/Final Visit Vaginal pH was obtained at final visit of the study. The pH was a numeric value from a scale of 0 to 14 expressing the acidity or alkalinity of the vaginal fluids where 7 was neutral, lower values were more acidic (values of 0-6) and higher values more alkaline (values of 8-14). A negative change from Baseline indicates improvement. Week 12/Final Visit is defined as the last available postbaseline assessment up to Week 12. Baseline (Day 0) to Week 12/Final Visit
Primary Change From Baseline in Percentage of Vaginal Superficial Cells to Week 12/Final Visit Vaginal wall smears were collected from each participant. The smears were sent to the central laboratory for analysis to determine the percentage of superficial cells. Week 12/Final Visit is defined as the last available postbaseline assessment up to Week 12. Baseline (Day 0) to Week 12/Final Visit
Primary Change From Baseline in Percentage of Vaginal Parabasal Cells to Week 12/Final Visit Vaginal wall smears were collected from each participant. The smears were sent to the central laboratory for analysis to determine the percentage of parabasal cells. Week 12/Final Visit is defined as the last available postbaseline assessment up to Week 12. Baseline (Day 0) to Week 12/Final Visit
Secondary Change From Baseline in Investigator's Assessment of Atrophy to Week 12 and Week 12/Final Visit Investigator's assessment of vaginal health was performed by visual inspection of the vagina with respect to atrophy scored on a 4-point scale where: 0= none, 1= mild, 2= moderate, or 3= severe. The negative change from Baseline indicates improvement. Week 12/Final Visit is defined as the last available postbaseline assessment up to Week 12. Baseline (Day 0) to Week 12 and Week 12/Final visit
Secondary Change From Baseline in Investigator's Assessment of Pallor to Week 12 and Week 12/Final Visit Investigator's assessment of vaginal health was performed by visual inspection of the vagina with respect to pallor scored on a 4-point scale where: 0= none, 1= mild, 2= moderate, or 3= severe. The negative change from Baseline indicates improvement. Week 12/Final Visit is defined as the last available postbaseline assessment up to Week 12. Baseline (Day 0) to Week 12 and Week 12/Final visit
Secondary Change From Baseline in Investigator's Assessment of Vaginal Dryness to Week 12 and Week 12/Final Visit Investigator's assessment of vaginal health was performed by visual inspection of the vagina with respect to vaginal dryness scored on a 4-point scale where: 0= none, 1= mild, 2= moderate, or 3= severe. The negative change from Baseline indicates improvement. Week 12/Final Visit is defined as the last available postbaseline assessment up to Week 12. Baseline (Day 0) to Week 12 and Week 12/Final visit
Secondary Change From Baseline in Investigator's Assessment of Friability to Week 12 and Week 12/Final Visit Investigator's assessment of vaginal health was performed by visual inspection of the vagina with respect to friability scored on a 4-point scale where: 0= none, 1= mild, 2= moderate, or 3= severe. The negative change from Baseline indicates improvement. Week 12/Final Visit is defined as the last available postbaseline assessment up to Week 12. Baseline (Day 0) to Week 12 and Week 12/Final visit
Secondary Change From Baseline in Investigator's Assessment of Petechiae to Week 12 and Week 12/Final Visit Investigator's assessment of vaginal health was performed by visual inspection of the vagina with respect to petechiae scored on a 4-point scale where: 0= none, 1= mild, 2= moderate, or 3= severe. The negative change from Baseline indicates improvement. Week 12/Final Visit is defined as the last available postbaseline assessment up to Week 12. Baseline (Day 0) to Week 12 and Week 12/Final visit
Secondary Change From Baseline in Participant's Self-Assessment of Severity of Vaginal Dryness to Weeks 2, 4, 8 and 12 Participant's self-assessment of symptoms of VVA (severity of vaginal dryness) was scored according to a 4-point scale where: 0= none, 1= mild, 2= moderate, or 3= severe. The negative change from Baseline indicates improvement. Baseline (Day 0) to Weeks 2, 4, 8 and 12
Secondary Change From Baseline in Participant's Self-Assessment of Vaginal and/or Vulvar Irritation/Itching to Weeks 2, 4, 8, 12 and Week 12/Final Visit Participant's self-assessment of symptoms of VVA (vaginal and/or vulvar irritation/itching) was scored according to a 4-point scale where: 0= none, 1= mild, 2= moderate, or 3= severe. The negative change from Baseline indicates improvement. Week 12/Final Visit is defined as the last available postbaseline assessment up to Week 12. Baseline (Day 0) to Weeks 2, 4, 8, 12 and Week 12/Final visit
Secondary Change From Baseline in Participant's Self-Assessment of Dysuria (Painful or Difficult Urination) to Weeks 2, 4, 8, 12 and Week 12/Final Visit Participant's self-assessment of symptoms of VVA (dysuria) was scored according to a 4-point scale where: 0= none, 1= mild, 2= moderate, or 3= severe. The negative change from Baseline indicates improvement. Week 12/Final Visit is defined as the last available postbaseline assessment up to Week 12. Baseline (Day 0) to Weeks 2, 4, 8, 12 and Week 12/Final visit
Secondary Change From Baseline in Participant's Self-Assessment of Dyspareunia (Pain Associated With Sexual Activity) to Weeks 2, 4, 8, 12 and Week 12/Final Visit Participant's self-assessment of symptoms of VVA (dyspareunia) was scored according to a 4-point scale where: 0= none, 1= mild, 2= moderate, or 3= severe. The negative change from Baseline indicates improvement. Week 12/Final Visit is defined as the last available postbaseline assessment up to Week 12. Baseline (Day 0) to Weeks 2, 4, 8, 12 and Week 12/Final visit
Secondary Percentage of Participants With Vaginal Bleeding Associated With Sexual Activity as Per Participant's Self-Assessment to Weeks 2, 4, 8, 12 and Week 12/Final Visit Vaginal bleeding associated with sexual activity was assessed by participants as either "present" or "absent". Percentage of participants with assessment "present" are reported. Week 12/Final Visit is defined as the last available postbaseline assessment up to Week 12. Baseline (Day 0) and Weeks 2, 4, 8, 12 and Week 12/Final visit
Secondary Change From Baseline in Vaginal pH to Week 12 Vaginal pH was obtained at final visit of the study. The pH was a numeric value from a scale of 0 to 14 expressing the acidity or alkalinity of the vaginal fluids where 7 was neutral, lower values were more acidic (values of 0-6) and higher values more alkaline (values of 8-14). A negative change from Baseline indicates improvement. Baseline (Day 0) to Week 12
Secondary Change From Baseline in Percentage of Vaginal Superficial Cells to Week 12 Vaginal wall smears were collected from each participant. The smears were sent to the central laboratory for analysis to determine the percentage of superficial cells. Baseline (Day 0) to Week 12
Secondary Change From Baseline in Percentage of Vaginal Parabasal Cells to Week 12 Vaginal wall smears were collected from each participant. The smears were sent to the central laboratory for analysis to determine the percentage of parabasal cells. Baseline (Day 0) to Week 12
See also
  Status Clinical Trial Phase
Active, not recruiting NCT04982692 - A Clinical Study of Intravaginal Prasterone (Intrarosa®) in Postmenopausal Vulvovaginal Atrophy Phase 3
Recruiting NCT04657536 - Evaluating the Efficacy of Temperature-controlled Radiofrequency (TRF) in the Treatment of Vulvovaginal Atrophy. N/A