Clinical Trials Directory

Trials / Completed

CompletedNCT06670690

Comparison Between Atenolol,Propnalol and Ivabradine

Comparison Between Atenolol , Propnalol and Ivabradine as a Premedication for Bloodless Field Anesthesia in Lumbar Spine Surgery ,a Prospective Randomized Controlled Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
120 (actual)
Sponsor
Menoufia University · Academic / Other
Sex
All
Age
18 Years – 50 Years
Healthy volunteers
Accepted

Summary

The aim of this work is to compare atenolol, propranolol, and ivabradine as a premedication to achieve bloodless field anesthesia primarily controlling heart rate in lumbar spine surgery.

Detailed description

This study will investigate the effect of atenolol, propranolol, and ivabradine as oral premedication in adult patients undergoing LUMBAR SPINE SURGERY to achieve bloodless field anesthesia. AIM OF THE WORK * The primary aim of this work is to compare atenolol, propranolol, and ivabradine as a premedication to achieve bloodless field anesthesia primarily controlling heart rate in lumbar spine surgery. * The secondary aims are to assess field visibility and measure the amount of blood loss in patients, and surgeon satisfaction and also to asses if there are any associated undesirable side effects of atenolol, propranolol, or Ivabradine will appear.

Conditions

Interventions

TypeNameDescription
DRUGAtenolol 50 MGpatients will be premedicated with atenolol (50mg)
DRUGPropranolol Pillpatients will be premedicated with propranolol (10mg)
DRUGIvabradinepatients will be premedicated with Ivabradine (5mg)

Timeline

Start date
2023-09-01
Primary completion
2023-09-01
Completion
2023-10-01
First posted
2024-11-01
Last updated
2024-11-01

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT06670690. Inclusion in this directory is not an endorsement.