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Clinical Trials/NCT00449059
NCT00449059CompletedPhase 4

Acute Effect of Nitroglycerin on Cyclosporine-Induced Hypertension After Cardiac Transplantation

University of Zurich1 site in 1 country20 target enrollmentStarted: January 1, 2003Last updated:
Conditions
Drugs

Trial Snapshot

Phase
Phase 4
Status
Completed
Enrollment
20
Locations
1
Primary Endpoint
Blood pressure reduction after acute nitroglycerine infusion

Study Overview

Brief Summary

The aim of the study was to evaluate the acute effect of nitroglycerine infusion on blood pressure and heart rate in heart-transplanted patients with cyclosporine-induced hypertension.

Detailed Description

Background: Cyclosporine represents a milestone in immunosuppression after organ transplantation. Its use, however, comes at the cost of significant side effects, such as arterial hypertension. Our aim was to investigate the effect of acute administration of nitroglycerin in heart-transplanted patients with cyclosporine-induced hypertension.

Methods: We included 18 hypertensive patients (HT) scheduled for elective cardiac catheterization after heart transplantation and treated with cyclosporine, as well as 6-matched HT. Simultaneous measurements of BP in the aorta and pulmonary artery before and after administration of nitroglycerin were done.

Results: After injection of 50μg and 100μg nitroglycerin a significant BP decrease was observed both in heart-transplanted patients (sBP p=0.0001; dBP p=0.0001) and in controls (sBP p=0.006; dBP p=0.05). This reduction was more pronounced in heart-transplanted patients (sBP p=0.022; dBP 0.018 for group comparison). 8±3 minutes after the last nitrate infusion BP remained significantly reduced vs baseline in heart-transplanted patients (p<0.001) while it comes back to baseline in controls. The reduction in sBP (p=0.04 after 50μg nitroglycerin; p=0.05 after 100μg nitroglycerin) but not dBP correlated to cyclosporinemia.

Conclusions: This study indicates that nitroglycerin reduces sBP in heart-transplanted patients with cyclosporine-induced hypertension. Further studies are needed to evaluate the long-term effect of nitrates in these patients.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 80 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Heart-transplanted group:
  • •Patients with hypertension and treated with cyclosporine
  • •Patients under optimal standard therapy
  • •Patients giving written informed consent
  • •Control group:
  • •Patients with hypertension
  • •Patients without prior transplantation of any kind
  • •Patients giving written informed consent

Exclusion Criteria

  • •Hypertensive patients receiving immunosuppressive drugs
  • •Patients receiving any kind or nitrate derivates

Outcomes

Primary Outcomes

Blood pressure reduction after acute nitroglycerine infusion

Secondary Outcomes

  • Heart rate modification after acute nitroglycerine infusion

Investigators

Sponsor Class
Other

Study Sites (1)

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