Postmenopause Clinical Trial
Official title:
A Postmarketing Surveillance Study Evaluating the Tolerability and Safety of PREMARIN VAGINAL CREAM in Indian Postmenopausal Women
This post-marketing study will provide local safety and tolerance data on the use of Premarin® vaginal cream.
Status | Completed |
Enrollment | 200 |
Est. completion date | October 2006 |
Est. primary completion date | |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 40 Years to 65 Years |
Eligibility |
Inclusion Criteria: - Patients in whom Premarin vaginal cream is indicated. - In the opinion of the investigator, sufficient intelligence and motivation for the patient to continue throughout the study. - Provide signed informed consent. Exclusion Criteria: - Patients not willing to give informed consent. |
N/A
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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Wyeth is now a wholly owned subsidiary of Pfizer |
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