Effects of nebivolol on the cardiorespiratory parameters

Not Applicable

Recruiting

• Conditions: healthy.; Healthy person accompanying sick person; Z76.3

• Registration Number: IRCT20220603055064N1
• Lead Sponsor: Muhmmad institute of medical and allied sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 29 August 2022

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 200

Inclusion Criteria

Healthy female students
Mentally and physically fit
Normal BMI
Age 18-25

Exclusion Criteria

Menstruations period
Pregnant females
Lactating mother
Cardiac and respiratory issues
Surgery
Trauma

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Blood pressure. Timepoint: Participants were evaluated before and after giving medicine (Nebivolol). Method of measurement: Mercury manometer, Stethoscope, Stop watch, Mercury thermometer, Pulse oximeter.

Secondary Outcome Measures

Name	Time	Method
Endurance Quality of life improve. Timepoint: Before and After treatment. Method of measurement: with the help of questionnaire.