Skip to content

Evaluating the Outcome of Cardio Selective beta1- Blockers Use in Patients With Copd

Evaluating the Outcome of Cardio Selective beta1- Blockers Use in Patients With Chronic Obstructive Pulmonary Disease: A Pilot Study

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04845061
Enrollment
30
Registered
2021-04-14
Start date
2021-10-01
Completion date
2022-01-15
Last updated
2021-04-14

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

Conditions

Copd

Keywords

beta blockers -nebivolol

Brief summary

To Evaluate the Outcome of cardio selective beta1 (β1-) blockers use in patients with chronic obstructive pulmonary disease. Patient education about the COPD and their medications.

Detailed description

Chronic obstructive pulmonary disease (COPD) is a common preventable and Treatable airway disorder characterized by symptoms such as dyspnea, chronic Cough, and sputum production along with persistent airflow limitation that is not fully Reversible. Evidence provided by post hoc analysis of clinical trials and large observational studies suggests a beneficial effect of beta-blockers on mortality and exacerbation in mild to moderate COPD patients. Evidence concerning cardio selective B blockers. Over the past 20 years' non selective B blockers have largely been replaced with cardio selective blockers. Cardio selective beta blockers such as atenolol and metoprolol are at least 20 times more potent at blocking B-1 receptors than B-2 receptors. At therapeutic doses the B-1 blocking effect, and therefore the risk of bronco constriction, is negligible. In addition there is strong evidence that B-blocked cause up-regulation and sensitization of B-receptors.

Interventions

DRUGNebivolol Tablets

cardio selective beta-1 blocker

Sponsors

Ain Shams University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
PREVENTION
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
40 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

1. Male or female. 2. informed consent. 3. Age \>40years. 4. FEVl/FVC\<70%. 5. diagnosed 3 month before enrollment (mild-moderate) 6. Reversability test pre-post bronchodilators FEVl predicted\<200ml/hr and less than 12%.

Exclusion criteria

1. Asthmatic patient. 2. patient already use B blockers. 3. Acute exacerbation. 4. Pregnency -lactation. 5. Advanced cardiac, renal or liver disease according to investigator opinion.

Design outcomes

Primary

MeasureTime frameDescription
forced vital capacity3 monthsamount of air that can be forcibly exhaled from the lung after taking the deepest breath possible (FVC\\liter)
forced expiratory volume in one second3 monthvolume of air exhaled under condition in the first second (FEV1\\liter)
blood pressure3 monthBP millimetre mercury

Countries

Egypt

Contacts

Primary Contactasma suliman, bachelor
asma.shain2017@gmail.com00201006279989
Backup Contactmarwa adel, associated professor
dr.marwa.adel2016@gmail.com00201006383120

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026