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Efficacy and Tolerability in Thai Women - Article


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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

Sponsored by: Schering AG, Germany
Information provided by: Schering AG, Germany
ClinicalTrials.gov Identifier: NCT00185328

Purpose

To evaluate the safety, tolerability, and efficacy of Angeliq® in Thai post menopausal women with hot flushes and other climacteric symptoms.
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

Further Study Details: 
Primary Outcomes: This study aims to evaluate the safety, tolerability and efficacy of Angeliq® in Thai postmenopausal women with hot flushes and other climacteric and urogenital symptoms.

Study start: September 2005

Eligibility

Ages Eligible for Study:  45 Years and above,  Genders Eligible for Study:  Female
Criteria

Inclusion Criteria:

  • Postmenopausal women with hot flushes

Exclusion Criteria:

  • Women with a contraindication for HRT

Location and Contact Information

Please refer to this study by ClinicalTrials.gov identifier  NCT00185328

Schering AG, Germany, Medical affairs, Region Asia/ Pacific      +65 6511 6194 

Thailand
      Bangkok,  10330,  Thailand

      Bangkok,  10400,  Thailand

      Bangkok,  10700,  Thailand

      Chiang Mai,  50200,  Thailand

Study chairs or principal investigators

Schering AG, Germany, , Medical affairs, Region Asia/ Pacific,  Study Director,  +65 6511 6194   

More Information

Study ID Numbers:  309367
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

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November 18, 2008



Page Updated: June 1, 2005
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