Comparative Effects of Moxonidine on Bone Metabolism, Vascular and Cellular Aging in Hypertensive Postmenopausal Women
NCT02355821 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 114
Last updated 2021-09-01
Summary
This study evaluates the effect of moxonidine versus bisoprolol on collagen type 1 C-telopeptide in postmenopausal female patients with arterial hypertension and osteopenia.
Conditions
- Osteopenia
- Arterial Hypertension
Interventions
- DRUG
-
Moxonidine
0.4 mg moxonidine QD titration up to 0.6 mg moxonidine BID Other Names:perindopril 10 mg/day (optional); losartan 50 mg/day (optional); calcium carbonate; vitamin D
- DRUG
-
Bisoprolol
5 mg Bisoprolol QD titration up to 7.5 mg Bisoprolol BID Other Names: perindopril 10 mg/day (optional); losartan 50 mg/day (optional); calcium carbonate; vitamin D
Sponsors & Collaborators
-
National Research Center for Preventive Medicine
lead OTHER_GOV
Principal Investigators
-
Olga N Tkacheva, Professor · [email protected]
Study Design
- Allocation
- RANDOMIZED
- Purpose
- BASIC_SCIENCE
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Sex
- FEMALE
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2015-04-30
- Primary Completion
- 2018-06-15
- Completion
- 2018-07-10
Countries
- Russia
Study Locations
More Related Trials
-
Comparative Study of the Effects of Telmisartan and Nebivolol
NCT02057328 ·Status: UNKNOWN ·Phase: PHASE4
-
Comparing Bisoprolol and Valsartan-Amlodipine for Hypertension
NCT07327749 ·Status: COMPLETED ·Phase: PHASE4
-
To Evaluate Real-world Safety, Effectiveness and Appropriate Use of Micatrio® Combination Tablets Treatment in Patients With Hypertension
NCT03021265 ·Status: COMPLETED
-
The Effect of Moxonidine on Blood Pressure and Regression of Early Target Organ Damage in Young Subjects With Abdominal Obesity and Hypertension
NCT01360710 ·Status: UNKNOWN ·Phase: PHASE4
-
Evaluation of the Clinical Efficacy and Safety of Amlodipine 5mg/ Bisoprolol Fumarate 5mg /Perindopril Arginine 5mg Fixed-dose Combination in Capsule and Free Monotherapy at the Same Dose in Patients With Uncontrolled Essential Hypertension.
NCT05288400 ·Status: COMPLETED ·Phase: PHASE3
-
Bioequivalence Study of Telmisartan/Amlodipine Fixed Dose Combination Compared With Its Monocomponents in Healthy Male and Female Volunteers
NCT02259829 ·Status: COMPLETED ·Phase: PHASE1
-
Bioequivalence of Telmisartan/Amlodipine Fixed Dose Combination Compared With Its Monocomponents in Healthy Male and Female Volunteers
NCT02193308 ·Status: COMPLETED ·Phase: PHASE1
-
An Efficacy and Safety Study Evaluating the Fixed-Dose Combination of Candesartan Plus Amlodipine in Participants With Mild/Moderate Essential Hypertension
NCT02969265 ·Status: WITHDRAWN ·Phase: PHASE3
-
Pharmacodynamic Influences of Candesartan, Atenolol, Hydrochlorothiazide and Drug Combinations in Hypertensive Patients.
NCT00232882 ·Status: COMPLETED ·Phase: PHASE4
-
Study to Evaluate the Efficacy and Safety of Combined Administration of TAK-536CCB and Hydrochlorothiazide in Patients With Grade I or II Essential Hypertension.
NCT02072330 ·Status: COMPLETED ·Phase: PHASE2/PHASE3
-
The Effects of Antihypertensive Agents on Central Blood Pressure in Healthy Participants and Participants With Hypertension (MK-0000-166) (COMPLETED)
NCT01130168 ·Status: COMPLETED ·Phase: PHASE1
-
Study to Evaluate the Trough and Peak Effect of Once Daily Telmisartan 80 mg/Hydrochlorothiazide 12.5 mg (Micardis Plus) by Ambulatory Blood Pressure Monitoring (ABPM) in Patients With Mild to Moderate Essential Hypertension
NCT00257491 ·Status: COMPLETED ·Phase: PHASE3
-
Telmisartan+Amlodipine Fixed Dose Combination in Hypertension
NCT01204398 ·Status: COMPLETED ·Phase: PHASE3
-
Comparison of Tandospirone, Amlodipine and Their Combination in Adults With Hypertension and Anxiety
NCT03667677 ·Status: UNKNOWN ·Phase: PHASE4
-
Bioequivalence Study of Telmisartan Between Telmisartan 80 mg/Amlodipine 5 mg/Hydrochlorothiazide 12.5 mg (T80/A5/H12.5 mg) Fixed-dose Combination (FDC) Tablet and T80/H12.5 mg Tab and A5 mg (Encap A2.5 mg Tab x2) Concomitant Use
NCT02129192 ·Status: COMPLETED ·Phase: PHASE1
-
Bioequivalence Study of Telmisartan Between Telmisartan 80 mg/Amlodipine 5 mg FDC Tablet and Telmisartan 80 mg Tab and Amlodipine 5 mg Tab Concomitant Use
NCT01344629 ·Status: COMPLETED ·Phase: PHASE1
-
Relative Bioavailability of Telmisartan/Amlodipine Fixed-dose Combination Compared to Its Mono-components in Healthy Male Volunteers
NCT02259803 ·Status: COMPLETED ·Phase: PHASE1
-
Efficacy and Safety of Metoprolol Succinate Prolonged-Release Tablet in Patients With Mild to Moderate Hypertension
NCT00861016 ·Status: COMPLETED ·Phase: PHASE4
-
Telmisartan and Amlodipine Versus Monocomponent Tablets
NCT01278797 ·Status: COMPLETED ·Phase: PHASE1
-
Telmisartan Versus Amlodipine in Patients With Mild-to-Moderate Hypertension
NCT02177409 ·Status: COMPLETED ·Phase: PHASE3
-
Blood Pressure and Weight Trajectory on a Dual Antihypertensive Combination Plus Sibutramine Versus Placebo in Obese Hypertensives
NCT00679653 ·Status: COMPLETED ·Phase: PHASE3
-
Comparison of Blood Pressure Control Achieved in Antihypertensive or Generic Drugs in Moderate to Severe Hypertensive Patients
NCT02853045 ·Status: COMPLETED ·Phase: PHASE4
-
Comparision of Blood Pressure Variability Between Amlodipine and Losartan
NCT01964079 ·Status: COMPLETED ·Phase: PHASE4
-
Telmisartan Versus Losartan in Kidney Transplantation
NCT01224860 ·Status: COMPLETED ·Phase: PHASE2
-
Open Label Study Telmisartan and Amlodipine in Hypertension
NCT00614380 ·Status: COMPLETED ·Phase: PHASE3