Overview

Arginine Malaria Trial: Study of Adjunctive Arginine in Falciparum Malaria

Status:
Completed
Trial end date:
2007-12-01
Target enrollment:
0
Participant gender:
All
Summary
Acute falciparum malaria is associated with low plasma arginine and impaired nitric oxide (NO) production. Both are associated with poor outcome. This study will examine the safety and effect of escalating doses of arginine in falciparum malaria. It will determine whether arginine can increase NO production and have an effect on NO-dependent physiological measurements. The hypothesis is that arginine: will be safe in falciparum malaria; will return plasma arginine concentration to normal/supranormal levels; will increase systemic and exhaled NO; reduces oxidant stress; and improves a number of NO-dependent physiological measures of relevance to malaria.
Phase:
Phase 1/Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Menzies School of Health Research
Collaborators:
MSHR
National Health and Medical Research Council, Australia
National Institute of Health Research and Development, Ministry of Health Republic of Indonesia
Rumah Sakit Mitra Masyarakat Hospital
University of Sydney
University of Utah
Wellcome Trust
Criteria
Inclusion Criteria:

1. Ages 18-60 years

2. P. falciparum parasitemia (1,000-100,000 parasites/ul).

3. Clinical syndrome consistent with malaria associated with documented fever (axillary
temperature > 38℃) or self-reported history of fever in the last 48 hours with no
other cause present

4. Commenced oral quinine ≤ 18 hours prior to scheduled commencement of arginine

5. An indication for hospital admission (eg relative cannot look after/supervise
treatment at home but not having any warning signs or severe malaria criteria in
"exclusion criteria" below)

6. Informed consent obtained

Exclusion Criteria:

1. Pregnancy or lactation

2. Mixed infection with P. falciparum and P. vivax

3. Warning signs of altered mental state and inability to sit unaided

4. Features of severe/complicated malaria

5. Diabetes

6. Systolic blood pressure (BP) < 100 mmHg

7. Serious underlying disease (cardiac, hepatic, kidney)

8. Initial iSTAT test showing any of the following values:

- glucose < 4 mmol/L;

- K+ ≥ 4.2 meq/L;

- Cl- > 106 meq/L;

- HCO3- < 20 meq/L.

9. Known allergy to L-arginine

10. Concurrent therapy with any of the following medications:

- spironolactone;

- oral nitrates;

- phosphodiesterase inhibitor (eg sildenafil [Viagra]);

- alpha-blocking antihypertensive agents (eg prazosin);

- L-arginine.