Estradiol Vaginal Ring |
Estring; Femring |
Clinical Trial: Efficacy and Tolerability in Thai Women
This study is not yet open for patient recruitment.
Verified by Schering AG, Germany September 2005
|
Purpose
| Condition | Intervention |
|---|---|
| Menopause | Drug: Estradiol Drug: Drospirenone |
MedlinePlus consumer health information
Study Type: Interventional
Study Design: Treatment, Non-Randomized, Open Label, Uncontrolled, Parallel Assignment, Safety/Efficacy Study
Official Title: A Multi-Center, Open-Label, Non-Comparative Study Investigating the Efficacy and Tolerability of Angeliq® in Postmenopausal Thai Women with Vasomotor Symptoms Over Three 28-Day Treatment Cycles
Study start: September 2005
Eligibility
Inclusion Criteria:
- Postmenopausal women with hot flushes
Exclusion Criteria:
- Women with a contraindication for HRT
Location and Contact Information
Thailand
Bangkok, 10330, Thailand
Bangkok, 10400, Thailand
Bangkok, 10700, Thailand
Chiang Mai, 50200, Thailand
Schering AG, Germany, , Medical affairs, Region Asia/ Pacific, Study Director, +65 6511 6194
More Information
Last Updated: September 15, 2005
Record first received: September 12, 2005
ClinicalTrials.gov Identifier: NCT00185328
Health Authority: Thailand: Food and Drug Administration
ClinicalTrials.gov processed this record on 2005-09-20
Resources
- Estradiol Vaginal Ring (Drug Digest)
- Estring (Drug Digest)

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