Trials / Unknown
UnknownNCT02455960
Protective Effects of Oral L-Arginine CI-AKI
Protective Effects of Oral L-Arginine Supplement in Patients With CKD After Intravenous Contrast Media Injection
- Status
- Unknown
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 112 (estimated)
- Sponsor
- Phramongkutklao College of Medicine and Hospital · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Accepted
Summary
This trial was performed to examine the efficacy of oral L-arginine for preventing CI-AKI in chronic kidney disease (CKD) patients.
Detailed description
Contrast-induced acute kidney injury (CI-AKI) is a common complication in hospitalized patients. Nitric oxide-signal transduction plays an important role in prevention of CI-AKI. L-Arginine is an amino acid involved in ammonia detoxification, and is well known as a precursor to nitric oxide, a key component of endothelial-derived relaxing factor. This is a prospective randomized, double blind, placebo controlled trial among CKD stage 3-4 patients undergoing computer tomography. Eligible patients were randomly assigned to two groups: (1) arginine 3 g/day or 6 capsules per day, and (2) placebo 6 capsules per day for 3 days before contrast media injection. Serum cystatin C, serum creatinine and estimated GFR was measured at baseline and 48 hours after procedure.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DIETARY_SUPPLEMENT | L-arginine | Comparison of the efficacy of L-arginine 3 grams for days versus placebo in contrast induced AKI prevention |
| DIETARY_SUPPLEMENT | Placebo |
Timeline
- Start date
- 2014-09-01
- Primary completion
- 2016-04-01
- Completion
- 2016-05-01
- First posted
- 2015-05-28
- Last updated
- 2015-05-28
Locations
1 site across 1 country: Thailand
Source: ClinicalTrials.gov record NCT02455960. Inclusion in this directory is not an endorsement.