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Moxonidine Effects on Neuropeptide Y

NCT ID: NCT05147753

Last Updated: 2021-12-07

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE4

Total Enrollment

90 participants

Study Classification

INTERVENTIONAL

Study Start Date

2010-01-11

Study Completion Date

2014-06-30

Brief Summary

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

Detailed Description

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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

Conditions

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Obesity Hypertension

Keywords

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hypertension obesity Neuropeptide Y moxonidine

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Group

0.6 mg moxonidine daily

Group Type EXPERIMENTAL

Moxonidine

Intervention Type DRUG

0.6 mg moxonidine daily

Interventions

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Moxonidine

0.6 mg moxonidine daily

Intervention Type DRUG

Eligibility Criteria

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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,
Minimum Eligible Age

25 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Aristotle University Of Thessaloniki

OTHER

Sponsor Role lead

Responsible Party

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Prof. Triantafyllos Didangelos

Associate Professor of Internal Medicine-Diabetology

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Eleni Karlafti, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

AHEPA University Hospital

Other Identifiers

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7337_20042021

Identifier Type: -

Identifier Source: org_study_id