Clinical Trials Directory

Trials / Completed

CompletedNCT02355821

Comparative Effects of Moxonidine on Bone Metabolism, Vascular and Cellular Aging in Hypertensive Postmenopausal Women

Comparative Effects of Moxonidine and Bisoprolol on Bone Metabolism, Vascular and Cellular Markers of Aging, Blood Pressure in Hypertensive Postmenopausal Women (COMPASS)

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
114 (actual)
Sponsor
National Research Center for Preventive Medicine · Other Government
Sex
Female
Age
Healthy volunteers
Not accepted

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.

Detailed description

Several experimental studies have demonstrated that moxonidine may lower the activity of Na+- independent Cl-/bicarbonate exchanger (anion exchanger, AE) which plays an essential role in viability of osteoclasts that are crucial for bone resorption. The suppression of AE proteins activity has been proven to inhibit osteoclast activity and reduce bone resorption whereas the moxonidine molecule is known to reduce the AE protein activity. Therefore, the results of experimental studies have shown the ability of moxonidine to inhibit bone resorption through its effect on the osteoclast activity. Published data contain information on positive effects of beta-blockers on the bone tissue condition. There are data which clearly demonstrate a positive effect of beta-blockers on bone mass. The proposed trial is a comprehensive study of moxonidine effects on processes of cellular and vascular aging as well as bone metabolism.

Conditions

Interventions

TypeNameDescription
DRUGMoxonidine0.4 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
DRUGBisoprolol5 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

Timeline

Start date
2015-04-01
Primary completion
2018-06-15
Completion
2018-07-10
First posted
2015-02-04
Last updated
2021-09-01
Results posted
2021-09-01

Locations

1 site across 1 country: Russia

Source: ClinicalTrials.gov record NCT02355821. Inclusion in this directory is not an endorsement.