Hydroxychloroquine for post-exposure prophylaxis of COVID-19 among naval personnel in Sri Lanka: study protocol for a randomized, controlled trial

被引:4
作者
Niriella, Madunil A. [1 ]
Ediriweera, Dileepa S. [1 ]
De Silva, Arjuna P. [1 ]
Premarathne, Ranjan [1 ]
Balasooriya, Priyantha [2 ]
Duminda, Kaluthanthri D. [3 ]
Malavige, Neelika G. [4 ]
Wanigasuriya, Kamani [4 ]
Lekamwasam, Sarath [5 ]
Kularathne, Senanayake A. [6 ]
Siribaddana, Sisira [7 ]
de Silva, Hithanadura J. [1 ]
Jayasinghe, Saroj [8 ]
机构
[1] Univ Kelaniya, Fac Med, Ragama, Sri Lanka
[2] Navy Hosp, Welisara, Sri Lanka
[3] Army Hosp, Narahenpita, Sri Lanka
[4] Univ Sri Jayawardenapura, Fac Med Sci, Nugegoda, Sri Lanka
[5] Univ Ruhuna, Fac Med, Galle, Sri Lanka
[6] Univ Peradeniya, Fac Med, Kandy, Sri Lanka
[7] Rajarata Univ Sri Lanka, Fac Med & Allied Sci, Anuradhapura, Sri Lanka
[8] Univ Colombo, Fac Med, Colombo, Sri Lanka
关键词
Randomized controlled trial; COVID-19; SARS-CoV-2; Prophylaxis; Post-exposure; Hydroxychloroquine; HCQ; Sri Lanka; EFFICACY;
D O I
10.1186/s13063-020-04659-7
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: The first case of a coronavirus 2019 (COVID-19) infection in a Sri Lankan was reported on March 11, 2020. The situation in Sri Lanka changed with the rapid increase of personnel contracting COVID-19 in a naval base camp that housed more than 4000 people. This provided a unique opportunity to study the effectiveness of hydroxychloroquine (HCQ) for post-exposure prophylaxis (PEP), while taking stringent, non-pharmacologic, public health measures to prevent spread. Our aim is to study the effectiveness and safety of HCQ for PEP among naval personnel with exposure to COVID-19-positive patients. Methods/design: This is a placebo-controlled, randomized, clinical trial carried out in the naval base camp and quarantine centers of the Sri Lanka Navy, Ministry of Defense, Sri Lanka. Navy personnel who are exposed to a patient with confirmed COVID-19 infection but test negative for the virus on reverse real-time polymerase chain reaction (rRT-PCR) at recruitment will be randomized, 200 to each arm, to receive HCQ or placebo and monitored for the development of symptoms or rRT-PCR positivity for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) virus for 14 days. Discussion: This trial will provide high-quality evidence of the effectiveness and safety of HCQ as PEP for COVID-19. The study design is unique due to the circumstances of the outbreak in a confined area among otherwise healthy adults, at a relatively early stage of its spread.
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页数:6
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