ClinicalTrials.Veeva

Menu

Nutrient Levels Alter Transplant Outcome

University of Cincinnati logo

University of Cincinnati

Status

Completed

Conditions

Chronic Renal Disease

Treatments

Dietary Supplement: Coromega and Arginine
Dietary Supplement: Arginine and canola oil

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT00560014
5U01AI040167 (U.S. NIH Grant/Contract)
LIPIDS
R03 AI142743

Details and patient eligibility

About

The purpose of this study is to look at lipid profiles of plasma and RBC and amino acid profiles in plasma to determine if they are associated with allograft rejection, calcineurin inhibitor toxicity or new onset diabetes mellitus in renal transplant patients receiving dietary supplements with arginine and omega-3 fatty acids.

Enrollment

54 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Renal transplant recipient
  • Appropriate blood samples drawn and analyzed

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Factorial Assignment

Masking

None (Open label)

54 participants in 3 patient groups

1
Experimental group
Description:
Arginine and Canola oil supplemented group
Treatment:
Dietary Supplement: Arginine and canola oil
2
Experimental group
Description:
Arginine and Coromega
Treatment:
Dietary Supplement: Coromega and Arginine
3
No Intervention group
Description:
Control

Trial contacts and locations

2

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems