scholarly journals Successful Double‐Blinded, Randomized, Placebo‐Controlled Field Trial of Azithromycin and Doxycycline as Prophylaxis for Malaria in Western Kenya

1998 ◽  
Vol 26 (1) ◽  
pp. 146-150 ◽  
Author(s):  
S. L. Andersen ◽  
A. J. Oloo ◽  
D. M. Gordon ◽  
O. B. Ragama ◽  
G. M. Aleman ◽  
...  
2007 ◽  
Vol 35 (2) ◽  
pp. 41-45 ◽  
Author(s):  
Noboru Minakawa ◽  
George Sonye ◽  
Kyoko Futami ◽  
Satoshi Kaneko ◽  
Emmanuel Mushinzimana ◽  
...  

PLoS ONE ◽  
2014 ◽  
Vol 9 (10) ◽  
pp. e111195 ◽  
Author(s):  
Hitoshi Kawada ◽  
Gabriel O. Dida ◽  
Kazunori Ohashi ◽  
Emiko Kawashima ◽  
George Sonye ◽  
...  

Vaccine ◽  
2018 ◽  
Vol 36 (43) ◽  
pp. 6433-6441 ◽  
Author(s):  
Angela Toepp ◽  
Mandy Larson ◽  
Geneva Wilson ◽  
Tara Grinnage-Pulley ◽  
Carolyne Bennett ◽  
...  

2014 ◽  
Vol 28 (3) ◽  
pp. 861-866 ◽  
Author(s):  
MERCELYNE KHALUMBA ◽  
TOBIAS WüNSCHER ◽  
SVEN WUNDER ◽  
MIRJAM BüDENBENDER ◽  
KARIN HOLM-MüLLER

2021 ◽  
Author(s):  
Eric O. Ochomo ◽  
John E. Gimnig ◽  
Achuyt Bhattarai ◽  
Aaron M. Samuels ◽  
Simon Kariuki ◽  
...  

Abstract Background: Spatial repellents are widely used for prevention of mosquito bites and evidence is building on their public health value, but their efficacy against malaria incidence has never been evaluated in Africa. To address this knowledge gap, a trial to evaluate the efficacy of Mosquito Shield™, a spatial repellent incorporating transfluthrin, was developed for implementation in Busia County, western Kenya where long-lasting insecticidal net coverage is high and baseline malaria transmission is moderate to high year-round. Methods: This trial is designed as a cluster-randomized, placebo-controlled, double-blinded clinical trial. Sixty clusters will be randomly assigned in a 1:1 ratio to receive spatial repellent or placebo. A total of 6120 children aged ≥ 6 months to 10 years of age will be randomly selected from the study clusters, enrolled into an active cohort (baseline, cohort 1, and cohort 2), and sampled monthly to determine time to first infection by smear microscopy. Each cohort following the implementation of the intervention, will be split into two groups, one to estimate direct effect of the spatial repellent and the other to estimate degree of diversion of mosquitoes and malaria transmission to unprotected persons. Malaria incidence in each cohort will be estimated and compared (primary indicator) to determine benefit of using a spatial repellent in a high, year-round malaria transmission setting. Mosquitoes will be collected monthly using CDC light traps to determine if there are entomological correlates of spatial repellent efficacy that may be useful for the evaluation of new spatial repellents. Quarterly human landing catches will assess behavioral effects of the intervention. Discussion: Findings will serve as the first cluster-randomized controlled trial powered to detect spatial repellent efficacy to reduce malaria in sub-Saharan Africa where transmission rates are high, insecticide treated nets are widely deployed, and mosquitoes are resistant to insecticides. Results will be submitted to the World Health Organization Vector Control Advisory Group for assessment of public health value towards an endorsement to recommend inclusion of spatial repellents in malaria control programs. Trial registration: ClinicalTrials.gov NCT04766879. Registered February 23, 2021.


VASA ◽  
2017 ◽  
Vol 46 (6) ◽  
pp. 462-470 ◽  
Author(s):  
Gerald Hackl ◽  
Andreas Prenner ◽  
Philipp Jud ◽  
Franz Hafner ◽  
Peter Rief ◽  
...  

Abstract. Background: Auricular nerve stimulation has been proven effective in different diseases. We investigated if a conservative therapeutic alternative for claudication in peripheral arterial occlusive disease (PAD) via electroacupuncture of the outer ear can be established. Patients and methods: In this prospective, double-blinded trial an ear acupuncture using an electroacupuncture device was carried out in 40 PAD patients in Fontaine stage IIb. Twenty patients were randomized to the verum group using a fully functional electroacupuncture device, the other 20 patients received a sham device (control group). Per patient, eight cycles (1 cycle = 1 week) of electroacupuncture were performed. The primary endpoint was defined as a significantly more frequent doubling of the absolute walking distance after eight cycles in the verum group compared to controls in a standardized treadmill testing. Secondary endpoints were a significant improvement of the total score of the Walking Impairment Questionnaire (WIQ) as well as improvements in health related quality of life using the Short Form 36 Health Survey (SF-36). Results: There were no differences in baseline characteristics between the two groups. The initial walking distance significantly increased in both groups (verum group [means]: 182 [95 % CI 128–236] meters to 345 [95 % CI 227–463] meters [+ 90 %], p < 0.01; control group [means]: 159 [95 % CI 109–210] meters to 268 [95 % CI 182–366] meters [+ 69 %], p = 0.01). Twelve patients (60 %) in the verum group and five patients (25 %) in controls reached the primary endpoint of doubling walking distance (p = 0.05). The total score of WIQ significantly improved in the verum group (+ 22 %, p = 0.01) but not in controls (+ 8 %, p = 0.56). SF-36 showed significantly improvements in six out of eight categories in the verum group and only in one of eight in controls. Conclusions: Electroacupuncture of the outer ear seems to be an easy-to-use therapeutic option in an age of increasingly invasive and mechanically complex treatments for PAD patients.


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