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| Sponsor: | University of California, San Francisco |
|---|---|
| Collaborator: |
Ortho-McNeil, Inc. |
| Information provided by: | University of California, San Francisco |
| ClinicalTrials.gov Identifier: | NCT00357981 |
Purpose
Dr. Eleanor Drey in the Department of Obstetrics, Gynecology and Reproductive Sciences UCSF is conducting a study to examine the personal and economic impact of continuous use of ORTHO EVRA, the contraceptive patch, on menstrual related symptoms for women who report having severe menstrual related symptoms.
| Condition | Intervention |
|---|---|
|
Dysmenorrhea Menstruation Disturbances Menstruation Disorders |
Drug: ORTHO EVRA, the contraceptive patch |
| Study Type: | Interventional |
| Study Design: | Treatment, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment, Efficacy Study |
| Official Title: | Patient Experiences Using Evra for Management of Menstrual Related Symptoms. |
| Estimated Enrollment: | 30 |
30 adult women, 18-40 years of age, will be recruited to participate in a six month study. The focus of recruitment will be on women with menstrual-related symptoms who are currently working in physically demanding, low autonomous service jobs.
The approximate first two months of women's participation will be spent documenting baseline information about their health and well-being, work patterns and performance, and the economic impact of their menstruation. Subjects will then initiate two, two month intervals of continuous use of ORTHO EVRA.
Over this four month treatment period, subjects will document their health and well-being, work patterns and performance, and the economic impact of their menstruation while being treated with ORTHO EVRA. This will allow us to compare subjects' experiences pre- and post-treatment. The study's instruments will focus on eliciting information on the personal and economic costs of menstruation such as measuring time missed from work, changes in productivity and work satisfaction, and impact on quality of life.
Eligibility| Ages Eligible for Study: | 18 Years to 40 Years |
| Genders Eligible for Study: | Female |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| United States, California | |
| UCSF/MZ Women's Health | |
| San Francisco, California, United States, 94110 | |
| Principal Investigator: | Eleanor Drey, MD, EdM | University of California, San Francisco |
More Information
| Study ID Numbers: | H10857-25721-01 |
| Study First Received: | July 26, 2006 |
| Last Updated: | May 19, 2008 |
| ClinicalTrials.gov Identifier: | NCT00357981 History of Changes |
| Health Authority: | United States: Food and Drug Administration |
|
Contraceptive patch menstruation economics |
|
Contraceptive Agents Contraceptives, Oral Physiological Effects of Drugs Contraceptive Agents, Female Pain Reproductive Control Agents Pharmacologic Actions Contraceptives, Oral, Combined |
Signs and Symptoms Pathologic Processes Pelvic Pain Dysmenorrhea Menstruation Disturbances Therapeutic Uses Ortho Evra |