Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07451522

Comparative Analysis of Analgesic Approaches in the Early Period After CABG

Comparative Characteristics of Analgesia Methods in the Early Postoperative Period After Coronary Artery Bypass Grafting (CABG)

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
100 (estimated)
Sponsor
Primorsky Regional General Hospital #1 · Other Government
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

The goal of this clinical trial is to study postoperative analgesia in patients undergoing CABG. And learn if tafalgin (tyrosyl-D-arginyl-phenylalanyl-glycine amid) treats pain not inferiory then morphine. The main questions it aims to answer are: Does tafalgin (tyrosyl-D-arginyl-phenylalanyl-glycine amid) lower the VAS score same way as a morphine? What medical problems do participants have when taking tafalgin (tyrosyl-D-arginyl-phenylalanyl-glycine amid)? Participants will: Group (1)- subcutaneous single dose of morphine 10 mg would be administred based on VAS score \> 3 during 24 hours after CABG. Exprimental group (2)- subcutaneous single dose of tafalgin (tyrosyl-D-arginyl-phenylalanyl-glycine amid) - 0.4 mg would be administred based on VAS score \> 3 during 24 hours after CABG. Efficacy was assessed using the VAS scale decreassion. Hemodynamic parameters and arterial blood gases were also assessed.

Conditions

Interventions

TypeNameDescription
DRUGTafalgin (tyrosyl-D-arginyl-phenylalanyl-glycine amide)Postoperative analgesia after CABG with tafalgin
DRUGMorphine (+)Postoperative analgesia wtih morphine

Timeline

Start date
2025-12-01
Primary completion
2026-03-01
Completion
2026-03-15
First posted
2026-03-05
Last updated
2026-03-05

Locations

1 site across 1 country: Russia

Source: ClinicalTrials.gov record NCT07451522. Inclusion in this directory is not an endorsement.