Moxonidine
Drug0.6 mg moxonidine daily
NCT Number: NCT05147753
Treatment with monotherapy of moxonidine 0.6 mg daily in treatment-naïve subjects with mild or moderate hypertension
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Notify Me25 year–75 year
All sexes
Interventional
Phase 4
Treatment with 0.6 mg moxonidine daily in treatment-naïve subjects with mild or moderate hypertension according to guidelines (Stage 1: Systolic Blood Pressure =140-159 mmHg, Diastolic Blood Pressure =90-99 mmHg, and Stage 2: systolic blood pressure=160-179 mmHg, diastolic blood pressure=100-109 mmHg) that require monotherapy and reevaluation after 12 weeks
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
0.6 mg moxonidine daily
Time frame: 12 weeks
ELISA
Time frame: 12 weeks
mmHg
Time frame: 12 weeks
mmHg
Time frame: 12 weeks
kg
Time frame: 12 weeks
kg/m2
Time frame: 12 weeks
mg/dl
Time frame: 12 weeks
mg/dl
Time frame: 12 weeks
mg/dl
Time frame: 12 weeks
mg/dl
Aristotle University Of Thessaloniki
Other
Effects of Moxonidine Administration on Serum Neuropeptide Y Levels in Hypertensive Individuals: A Prospective Observational Study
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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