Trials / Completed
CompletedNCT05147753
Moxonidine Effects on Neuropeptide Y
Effects of Moxonidine Administration on Serum Neuropeptide Y Levels in Hypertensive Individuals: A Prospective Observational Study
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 90 (actual)
- Sponsor
- Aristotle University Of Thessaloniki · Academic / Other
- Sex
- All
- Age
- 25 Years – 75 Years
- Healthy volunteers
- Not accepted
Summary
Treatment with monotherapy of moxonidine 0.6 mg daily in treatment-naïve subjects with mild or moderate hypertension
Detailed description
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
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Moxonidine | 0.6 mg moxonidine daily |
Timeline
- Start date
- 2010-01-11
- Primary completion
- 2014-06-30
- Completion
- 2014-06-30
- First posted
- 2021-12-07
- Last updated
- 2021-12-07
Source: ClinicalTrials.gov record NCT05147753. Inclusion in this directory is not an endorsement.