Trials / Completed
CompletedNCT01070940
L-NMMA Dose-response Study in Healthy Subjects
L-NMMA's Effect on Renal and Cardiovascular Variables in Healthy Subjects. A Randomized, Placebo-controlled Crossover Study.
- Status
- Completed
- Phase
- Phase 1
- Study type
- Interventional
- Enrollment
- 12 (actual)
- Sponsor
- Regional Hospital Holstebro · Academic / Other
- Sex
- Male
- Age
- 18 Years – 35 Years
- Healthy volunteers
- Accepted
Summary
The purpose of this study is to investigate the effect of different levels of nitric oxide inhibition on blood pressure and arterial stiffness in healthy subjects. L-NMMA, an inhibitor of the nitric oxide synthase, is administered as bolus injection followed by continuous infusion, and is expected to raise blood pressure and arterial stiffness according to L-NMMA dose.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | NG-monomethyl-L-arginine (L-NMMA) | 3 mg/kg IV priming dose + 2 mg/kg/hr IV infusion for 1 hour |
| DRUG | NG-monomethyl-L-arginine (L-NMMA) | 6 mg/kg IV priming dose + 4 mg/kg/hr IV infusion for 1 hour |
| DRUG | NG-monomethyl-L-arginine (L-NMMA) | 4.5 mg/kg IV priming dose + 3 mg/kg/hr IV infusion for 1 hour |
| DRUG | Placebo | Isotonic saline solution IV priming dose + IV infusion for 1 hour |
Timeline
- Start date
- 2010-02-01
- Primary completion
- 2010-06-01
- Completion
- 2010-06-01
- First posted
- 2010-02-18
- Last updated
- 2011-02-21
Locations
1 site across 1 country: Denmark
Source: ClinicalTrials.gov record NCT01070940. Inclusion in this directory is not an endorsement.