A Phase 3, Randomized, Three-Cycle, Double-Blind, Placebo-Controlled Study to Evaluate Induction of Secretory Conversion of Endometrium and Withdrawal Bleeding for Secondary Amenorrhea

PHASE3TerminatedINTERVENTIONAL
Enrollment

6

Participants

Timeline

Start Date

January 20, 2014

Primary Completion Date

October 31, 2014

Study Completion Date

October 31, 2014

Conditions
Secondary Amenorrhea
Interventions
DRUG

Progesterone

DRUG

Placebo

Trial Locations (22)

11777

Suffolk OBGYN, Port Jefferson

23456

Tidewater Clinical Research, Virginia Beach

27103

Lyndhurst Clinical Research, Winston-Salem

27615

Wake Research Associates, Raleigh

29201

Vista Clinical Research, Columbia

33409

Comprehensive Clinical Trials, LLC, West Palm Beach

34429

Nature Coast Clinical Research, Crystal River

37404

Chattanooga Medical Research, Chattanooga

45229

University of Cincinnati Physicians Company, Cincinnati

45322

HWC Women's Research Center, Englewood

67226

Cypress Medical Research Center, Wichita

68510

Women's Clinic of Lincoln, P.C., Lincoln

75115

Methodist Charlton Medical Center, DeSoto

77054

The Woman's Hospital of Texas Clinical Research Center, Houston

84070

PRO/Salt Lake Women's Center, Sandy City

85032

Precision Clinical Trials/Arizona Wellness Center for Women, Phoenix

85224

Precision Trials/New Horizons Women's Care, Chandler

85712

Visions Clinical Research, Tucson

90010

California Family Health Council, Los Angeles

94710

California Family Health Council, Berkeley

06460

Clinical Research Consulting, Milford

08648

Lawrence OB-Gyn Clinical Research, Lawrenceville

Sponsors

Lead Sponsor

All Listed Sponsors
lead

TherapeuticsMD

INDUSTRY

NCT02019589 - A Phase 3, Randomized, Three-Cycle, Double-Blind, Placebo-Controlled Study to Evaluate Induction of Secretory Conversion of Endometrium and Withdrawal Bleeding for Secondary Amenorrhea | Biotech Hunter | Biotech Hunter