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| Sponsored by: |
FDA Office of Orphan Products Development |
| Information provided by: | FDA Office of Orphan Products Development |
| ClinicalTrials.gov Identifier: | NCT00029731 |
Purpose
This is a study to determine if oral arginine will increase nitric oxide in sickle cell disease (SCD) patients with acute chest syndrome (ACS). It will also assess the effects of arginine in the body and how the body uses nitric oxide in ACS.
| Condition | Intervention | Phase |
|
Anemia, Sickle Cell Pneumonia |
Drug: Arginine hydrochloride |
Phase II |
| Genetics Home Reference related topics: | sickle cell disease |
| MedlinePlus related topics: | Anemia Pneumonia Sickle Cell Anemia |
| Drug Information available for: | Nitric oxide Arginine Arginine hydrochloride |
| Study Type: | Interventional |
| Study Design: | Treatment, Non-Randomized, Uncontrolled, Parallel Assignment, Efficacy Study |
| Official Title: | Arginine Therapy for Acute Chest Syndrome in Sickle Cell Disease |
| Estimated Enrollment: | 30 |
| Study Start Date: | August 2001 |
| Estimated Study Completion Date: | July 2004 |
Pneumonia in patients with SCD can be particularly severe and has come to be called acute chest syndrome. ACS is a common cause of morbidity in SCD patients and is the most common cause of death in SCD. Multiple factors are involved in the severity of acute pulmonary injury in SCD. Nitric oxide has a multitude of related functions, many of which could impact favorably on ACS in SCD. Nitric oxide is an important inflammatory mediator which is produced by the conversion of L-arginine to citrulline by nitric oxide synthase. Nitric oxide and its precursor, arginine, are known to be low in SCD patients with ACS, suggesting that therapies, such as arginine, aimed at increasing nitric oxide production will improve the clinical course of ACS. Patients will receive 1 of 3 doses of arginine hydrochloride orally 3 times a day for 3 days while hospitalized. The efficacy of arginine will be measured by the increase in nitric oxide production and the physiological effects will be assessed.
Eligibility
| Ages Eligible for Study: | 5 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion criteria:
Acute chest syndrome with the following:
Exclusion criteria:
Contacts and Locations| United States, California | |||||
| Children's Hospital Oakland | Recruiting | ||||
| Oakland, California, United States, 94609 | |||||
| Contact: Lori A. Styles, M.D. 510-428-3553 lstyles@mail.cho.org | |||||
| Principal Investigator: Lori A. Styles, M.D. | |||||
More Information
| Study ID Numbers: | FD-R-1978-01, FD-R-001978-01 |
| First Received: | January 21, 2002 |
| Last Updated: | June 23, 2005 |
| ClinicalTrials.gov Identifier: | NCT00029731 |
| Health Authority: | United States: Food and Drug Administration |
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