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A clinical trial to study the effect of one drug, Nebivolol on blood vessels in patients with high blood pressure

AN OPEN LABELLED EFFICACY AND TOLERABILITY STUDY OF NOVEL BETA-1- BLOCKER , NEBIVOLOL, ON HYPERTENSION WITH SPECIAL REFERENCE TO ENDOTHELIAL FUNCTION AND ARTERIAL STIFFNESS.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2012/02/002463
Enrollment
50
Registered
2012-02-28
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: null- Stage I Hypertension JNC7 Criteria

Interventions

Intervention1: Nebivolol: 5mg Once Daily for 15 days Control Intervention1: none: nil

Sponsors

Nizams Institute of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ) Ambulatory, Male and Female Volunteers between 18-55 years of age with a Body Mass Index (BMI) of approximately 18-30 kg/m2 diagnosed with stageI hypertension Essential Hypertension of greater than at least 1 month duration. 4) Stage 1 Hypertension with Systolic BP 140-159 or Diastolic BP 90-99 (JNC-7 Criteria) of greater than at least 1 month duration

Exclusion criteria

Exclusion criteria: 1) Secondary Hypertension. 2) Uncontrolled Hypertension. 3) History of Hypersensitivity to Beta Blockers or any component of the product. 4) Patients With Severe Bradycardia, Heart Block, Cardiogenic Shock, Decompensated Heart Failure, Sick Sinus Syndrome. 5) Females who are Pregnant or Lactating or planning to become Pregnant. 8) Subjects on Fluoxetine, Nicardipine, Cimetidine, Non- Dihydropyridine CCB?s and other CYP2D6 Inhibitors.

Design outcomes

Primary

MeasureTime frame
Central Aortic Pressures Timepoint: At baseline and End of treatment

Secondary

MeasureTime frame
Brachial blood pressure Carotid-Femoral pulse wave velocity Reflection Index & Stiffness index Ambulatory blood Pressure Timepoint: At baseline and end of treatment

Countries

India

Contacts

Public ContactDrRadhikaSoanker

Nizams Institute of Medical Sciences

raoramesh56@gmail.com9391049846

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026