Asthma Clinical Trial
Official title:
Exploratory Study of Lipoic Acid Supplementation on Oxidative Stress, Inflammatory and Functional Markers in Asthmatic Patients: Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Clinical Trial.
The aim of the study is to use the antioxidant and antiinflammatory effects of lipoic acid
to improve the quality of life of patients with asthma.
The investigators will administrate 600 mg lipoic acid orally on a daily basis during two
months concurrent with the patient anti-asthmatic therapy and evaluate the effects on
resulting pulmonary function, inflammatory and oxidative stress biomarkers and
health-related quality of life previous to the initial of the treatment and at 60 days of
the supplementary therapy.
Asthma is an inflammatory disease of high prevalence around the world. During development of
asthma the presence of oxidative stress has been related to susceptibility and severity of
the disease, thus making the use of antioxidant adjuvant therapy with lipoic acid (LA) an
interesting treatment option. The objective of the study is to evaluate the efficacy of LA
as an adjuvant treatment on functional, antioxidant, inflammatory, quality and control
parameters of asthma in human subjects. The trial design is a randomized, double blind,
placebo controlled parallel study.
Adult patients (>18 years) with history of mild intermittent to moderate asthma according to
the Global Initiative for Asthma (GINA) guidelines were enrolled. It was required a positive
skin prick test (>3 mm) for at least two regional allergens. Patients were randomly assigned
to receive lipoic acid or placebo for 60 days. Participants had an intermediate visit to the
attending physician one month after initial of treatment to monitor adverse events and to
undergo laboratory tests.
1. Introduction. Asthma is an inflammatory disease of high prevalence around the world.
During development of asthma the presence of oxidative stress has been related to
susceptibility and severity of the disease, thus making the use of antioxidant adjuvant
therapy with lipoic acid (LA) an interesting treatment option.
2. Study design. A randomized, double blind, placebo controlled parallel study
3. Methods. Participants and interventions: 55 patients with mild to moderate asthma from
Hospital Civil "Juan I. Menchaca" in Guadalajara, Jalisco, México were included and
randomized in block of 10 to receive; LA (600 mg/day) or placebo for eight weeks from
January to October of 2011.
4. Objective. To evaluate the efficacy of LA as an adjuvant treatment on functional,
antioxidant, inflammatory, quality and control parameters of asthma in human subjects.
Primary outcome: change on Forced expiratory volume in 1 second (FEV1), secondary
outcomes were levels of Oxygen radical absorbance capacity (ORAC), glutathione (GSH),
glutathione disulfide (GSSG), protein carbonyls, differential count of sputum cells,
interleukin-4 (IL-4) and scores of quality of life and control of asthma
questionnaires.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Supportive Care
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