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A Randomized, Double-Blind, Placebo-Controlled Trial of Lessertia frutescens in Healthy Adults
OBJECTIVES: Indigenous medicines are widely used throughout Africa, despite a lack of scientific evidence for their safety or efficacy. The aims of this study were: (a) to conduct a pilot study of the safety of a common indigenous South African phytotherapy, Lessertia frutescens (Sutherlandia), in h...
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2007
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1863514/ https://www.ncbi.nlm.nih.gov/pubmed/17476314 http://dx.doi.org/10.1371/journal.pctr.0020016 |
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author | Johnson, Quinton Syce, James Nell, Haylene Rudeen, Kevin Folk, William R |
author_facet | Johnson, Quinton Syce, James Nell, Haylene Rudeen, Kevin Folk, William R |
author_sort | Johnson, Quinton |
collection | PubMed |
description | OBJECTIVES: Indigenous medicines are widely used throughout Africa, despite a lack of scientific evidence for their safety or efficacy. The aims of this study were: (a) to conduct a pilot study of the safety of a common indigenous South African phytotherapy, Lessertia frutescens (Sutherlandia), in healthy adults; and (b) to contribute to establishing procedures for ethical and scientifically rigorous clinical trials of African indigenous medicines. DESIGN: A randomized, double-blind, placebo-controlled trial of Sutherlandia leaf powder in healthy adults. SETTING: Tiervlei Trial Centre, Karl Bremer Hospital, Bellville, South Africa. PARTICIPANTS: 25 adults who provided informed consent and had no known significant diseases or allergic conditions nor clinically abnormal laboratory blood profiles during screening. INTERVENTION: 12 participants randomized to a treatment arm consumed 400 mg capsules of Sutherlandia leaf powder twice daily (800 mg/d). 13 individuals randomized to the control arm consumed a placebo capsule. Each participant received 180 capsules for the trial duration of 3 mo. OUTCOME MEASURES: The primary endpoint was frequency of adverse events; secondary endpoints were changes in physical, vital, blood, and biomarker indices. RESULTS: There were no significant differences in general adverse events or physical, vital, blood, and biomarker indices between the treatment and placebo groups (p > 0.05). However, participants consuming Sutherlandia reported improved appetite compared to those in the placebo group (p = 0.01). Although the treatment group exhibited a lower respiration rate (p < 0.04) and higher platelet count (p = 0.03), MCH (p = 0.01), MCHC (p = 0.02), total protein (p = 0.03), and albumin (p = 0.03), than the placebo group, these differences remained within the normal physiological range, and were not clinically relevant. The Sutherlandia biomarker canavanine was undetectable in participant plasma. CONCLUSION: Consumption of 800 mg/d Sutherlandia leaf powder capsules for 3 mo was tolerated by healthy adults. |
format | Text |
id | pubmed-1863514 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-18635142007-05-02 A Randomized, Double-Blind, Placebo-Controlled Trial of Lessertia frutescens in Healthy Adults Johnson, Quinton Syce, James Nell, Haylene Rudeen, Kevin Folk, William R PLoS Clin Trials Research Article OBJECTIVES: Indigenous medicines are widely used throughout Africa, despite a lack of scientific evidence for their safety or efficacy. The aims of this study were: (a) to conduct a pilot study of the safety of a common indigenous South African phytotherapy, Lessertia frutescens (Sutherlandia), in healthy adults; and (b) to contribute to establishing procedures for ethical and scientifically rigorous clinical trials of African indigenous medicines. DESIGN: A randomized, double-blind, placebo-controlled trial of Sutherlandia leaf powder in healthy adults. SETTING: Tiervlei Trial Centre, Karl Bremer Hospital, Bellville, South Africa. PARTICIPANTS: 25 adults who provided informed consent and had no known significant diseases or allergic conditions nor clinically abnormal laboratory blood profiles during screening. INTERVENTION: 12 participants randomized to a treatment arm consumed 400 mg capsules of Sutherlandia leaf powder twice daily (800 mg/d). 13 individuals randomized to the control arm consumed a placebo capsule. Each participant received 180 capsules for the trial duration of 3 mo. OUTCOME MEASURES: The primary endpoint was frequency of adverse events; secondary endpoints were changes in physical, vital, blood, and biomarker indices. RESULTS: There were no significant differences in general adverse events or physical, vital, blood, and biomarker indices between the treatment and placebo groups (p > 0.05). However, participants consuming Sutherlandia reported improved appetite compared to those in the placebo group (p = 0.01). Although the treatment group exhibited a lower respiration rate (p < 0.04) and higher platelet count (p = 0.03), MCH (p = 0.01), MCHC (p = 0.02), total protein (p = 0.03), and albumin (p = 0.03), than the placebo group, these differences remained within the normal physiological range, and were not clinically relevant. The Sutherlandia biomarker canavanine was undetectable in participant plasma. CONCLUSION: Consumption of 800 mg/d Sutherlandia leaf powder capsules for 3 mo was tolerated by healthy adults. Public Library of Science 2007-04-27 /pmc/articles/PMC1863514/ /pubmed/17476314 http://dx.doi.org/10.1371/journal.pctr.0020016 Text en © 2007 Johnson et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Johnson, Quinton Syce, James Nell, Haylene Rudeen, Kevin Folk, William R A Randomized, Double-Blind, Placebo-Controlled Trial of Lessertia frutescens in Healthy Adults |
title | A Randomized, Double-Blind, Placebo-Controlled Trial of Lessertia frutescens in Healthy Adults |
title_full | A Randomized, Double-Blind, Placebo-Controlled Trial of Lessertia frutescens in Healthy Adults |
title_fullStr | A Randomized, Double-Blind, Placebo-Controlled Trial of Lessertia frutescens in Healthy Adults |
title_full_unstemmed | A Randomized, Double-Blind, Placebo-Controlled Trial of Lessertia frutescens in Healthy Adults |
title_short | A Randomized, Double-Blind, Placebo-Controlled Trial of Lessertia frutescens in Healthy Adults |
title_sort | randomized, double-blind, placebo-controlled trial of lessertia frutescens in healthy adults |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1863514/ https://www.ncbi.nlm.nih.gov/pubmed/17476314 http://dx.doi.org/10.1371/journal.pctr.0020016 |
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