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Table 1 Summary of chemoprophylaxis study design features

From: Chemoprophylaxis trial designs in epidemics: insights from a systematic review of COVID-19 study registrations

Trial characteristics

Number of trials (%), n = 76

Number proposed to be enrolled (%); total, 208,367

Median (IQR)

Design and intervention

Randomisation

 Randomised

Total

63(83)

197,010 (95)

600 (236–1834)

Cluster randomised

8(11)

12,710 (6)

1575 (1050–2075)

 Non-randomised

13 (17)

11,357 (5)

400 (300–1000)

Approach

 PrEP

55(72)

180,848 (87)

440 (203–1500)

 PEP

21(28)

27,519 (13)

1000 (400–2000)

Blinding

 Single-blinded

10 (13)

  

 Double-blinded

36(47)

 Open-label

28 (37)

 Not stated

2 (3)

Estimated sample size (N)

 ≤ 299

18 (24)

  

 300–499

20(26)

 500–999

7 (9)

 1000–4999

26 (34)

 5000+

5 (7)

Agent

 “Western” pharmaceutical agents

67 (88)

  

 TCM/ayurvedic

9(12)

Population

HCW

49 (64)

160,398 (77)

450 (350–1212)

Close contacts of COVID-19 patients

11 (14)

11,326 (5)

600 (293–1410)

Both HCW and close contacts

5 (7)

9625 (5)

2000 (1739–2486)

Older adults (65+ years)

3 (4)

2736 (1)

600 (403–1265)

General population

2 (3)

22,000 (11)

11,000 (6500–15,500)

Children (1–18 years)

1 (1)

200 (<1)

N/A

Other/unspecified (includes cancer, transplant and haemodialysis patients, cardiovascular/respiratory co-morbidities)

5 (7)

2132 (1)

200 (132–200)

  1. Also includes variants reporting higher levels of blinding