Validation Study for Endometriosis PRO

CompletedOBSERVATIONAL
Enrollment

275

Participants

Timeline

Start Date

August 31, 2012

Primary Completion Date

July 31, 2013

Study Completion Date

September 30, 2013

Conditions
Endometriosis
Interventions
OTHER

No drug

Patients with expected stable endometriosis management status (EMS), i.e. patients who have not planned a change in endometriosis treatment or a therapeutic surgical procedure in the next 12 weeks and have had no change in endometriosis treatment or therapeutic surgical procedure in the previous 4 weeks.lease specify as free-text; for drugs include daily dose, dosage form dosage frequency and duration (if appl. and possible for the OS/NIS).

OTHER

No drug

Patients with expected change in endometriosis management status (EMS), i.e. patients who have planned a change in endometriosis treatment or a therapeutic surgical procedure during the next 12 weeks or have undergone a change in endometriosis treatment or a therapeutic surgical procedure in the previous 4 weeks.

Trial Locations (21)

11203

Brooklyn

19104

Philadelphia

23502

Norfolk

27408

Greensboro

30034

Decatur

45242

Cincinnati

55905

Rochester

61820

Champaign

72401

Jonesboro

76904

San Angelo

84070

Sandy City

84107

Salt Lake City

92103

San Diego

92108

San Diego

94102

San Francisco

95816

Sacramento

97239

Portland

98105

Seattle

06511

New Haven

01655

Worcester

Unknown

Many Locations

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Bayer

INDUSTRY