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Effect of Nebivolol on climacteric disorders in postmenopausal women: A pilot study

Conditions
postmenopausal women
Registration Number
EUCTR2009-011527-31-AT
Lead Sponsor
Medizinische Universität Wien, Univ.Klinik KIM II, Abteilung für Kardiologie
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Recruiting
Sex
Female
Target Recruitment
60
Inclusion Criteria

•Menopausal patients (estrogen <20 pg/ml and FSH >35 mIU/ml)
•The patients are sexually active
•The patients have hot flushes
•The patients have palpitations or extrasystoles

Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

•Patients with COPD
•Patients with an AV-block
•Patients with a bradycardia (meaning a heart rate <50 beats per minute)
•Patients with hypotension (RR <100/80 mmHg)
•Patients with a PAD (stage III, IV)
•Patients with Asthma
•Patients with Morbus Raynaud
•Patients with a carcinoma
•Patients, who have already been treated because of hypertension
•Patients, who receive hormone replacement therapy

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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