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Completed

NCT Number: NCT05147753

Moxonidine Effects on Neuropeptide Y

Treatment with monotherapy of moxonidine 0.6 mg daily in treatment-naïve subjects with mild or moderate hypertension

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Key information

About this study

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

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • treatment-naïve subjects with mild or moderate hypertension according to Joint National Committee 7 and European Society Hypertension / European Society Cardiology 2008 (Stage 1: Systolic Blood Pressure =140-159 mmHg, Diastolic Blood Pressure =90-99 mmHg, and Stage 2: Systolic=160-179 mmHg, Diastolic=100-109 mmHg) that require monotherapy

Exclusion criteria

  • age beyond 25-75 years,
  • not taking currently anti-hypertensive medication
  • not taking anti-diabetic or lipid lowering medication and other diseases or conditions that may influence blood pressure, heart rate and catecholamines' and Neuropeptide Y levels, including anemia, fever, stage III hypertension, coronary artery disease, recent (less than 6 months) myocardial infraction or stroke, heart failure, secondary hypertension, diabetes mellitus, abnormal thyroid status or other obesity-related endocrinopathies, pregnancy, kidney failure, alcohol abuse, malignancies, depression or other psychiatric illnesses, such as schizophrenia,

Treatment and study plan

Moxonidine

Drug

0.6 mg moxonidine daily

Primary outcomes

  1. serum Neuropeptide Y levels

    Time frame: 12 weeks

    ELISA

  2. systolic blood pressure

    Time frame: 12 weeks

    mmHg

  3. diastolic blood pressure

    Time frame: 12 weeks

    mmHg

Secondary outcomes

  1. Weight

    Time frame: 12 weeks

    kg

  2. Body Mass Index

    Time frame: 12 weeks

    kg/m2

  3. Total Cholesterol

    Time frame: 12 weeks

    mg/dl

  4. HDL Cholesterol

    Time frame: 12 weeks

    mg/dl

  5. LDL Cholesterol

    Time frame: 12 weeks

    mg/dl

  6. Serum triglycerides

    Time frame: 12 weeks

    mg/dl

Sponsors and collaborators

Lead sponsor

Aristotle University Of Thessaloniki

Other

Registry information

Official study title

Effects of Moxonidine Administration on Serum Neuropeptide Y Levels in Hypertensive Individuals: A Prospective Observational Study

Important dates

Study start
2010
Primary completion
2014
Study completion
2014
First posted
Dec 7, 2021
Registry last updated
Dec 7, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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