| Literature DB >> 16359401 |
Camilo J Acosta1, Claudia M Galindo, Mohammad Ali, Remon Abu Elyazeed, R Leon Ochiai, M Carolina Danovaro-Holliday, Anne-Laure Page, Vu Dinh Thiem, Yang Jin, Jin Kyung Park, Hyejon Lee, Mahesh K Puri, Bernard Ivanoff, Magdarina D Agtini, Rooswanti Soeharno, Cyrus H Simanjuntak, Narain H Punjabi, Do Gia Canh, Dipika Sur, Qamaruddin Nizami, Byomkesh Manna, Dong Bai-qing, Dang Duc Anh, Yang Honghui, Sujit Kumar Bhattacharya, Zulfikar Bhutta, Dang Duc Trach, Zhi-Yi Xu, Tikki Pang, Allan Donner, John D Clemens.
Abstract
Phase-III vaccine efficacy trials typically employ individually randomized designs intended to ensure that measurements of vaccine protective efficacy reflect only direct vaccine effects. As a result, decisions about introducing newly licensed vaccines into public health programmes often fail to consider the substantially greater protection that may occur when a vaccine is deployed in public health programmes, due to the combination of direct plus indirect vaccine protective effects. Vaccine total protection can be better evaluated with cluster randomized trials. Such a design was considered to generate policy relevant data to accelerate the rationale introduction of the licensed typhoid fever Vi polysaccharide (PS) vaccine in Asia by the Diseases of the Most Impoverished (DOMI) typhoid fever programme. The DOMI's programme multi-country study is one of the largest cluster randomized vaccine trials ever mounted in Asia, which includes approximately 200,000 individuals. Its main objective is to determine the effectiveness of a licensed Vi PS vaccine. The rationale and design of this study are discussed. Preliminary results are presented that determined the final planning of the trial before immunization. Important methodological and practical issues regarding vaccine cluster randomized designs are illustrated.Entities:
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Year: 2005 PMID: 16359401 DOI: 10.1111/j.1365-3156.2005.01517.x
Source DB: PubMed Journal: Trop Med Int Health ISSN: 1360-2276 Impact factor: 2.622