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. 2020 Jul 6;11:1274. doi: 10.3389/fimmu.2020.01274

Table 1.

Demographics and clinical characteristics of the sub-set of women who acquire HIV infections during the CAPRISA 004 trials (n = 48).

Characteristics All (n = 48) Tenofovir (n = 24) Placebo (n = 24) p value
Rural % (n) 58.3% (28) 58.3% (14) 58.3% (14) ns
Median age in years (IQR) 23 (22–25) 24 (22–28) 22 (22–23) ns
Median days PI at enrolment (IQR) 38 (24–65) 35 (27–63) 45 (23–65) ns
Median CD4 count (cells/μl) (IQR) 498 (434–655) 468 (444–569) 515 (433–685) ns
Median viral load (copies/ml) (IQR) 59,0505 80,600 54.800 ns
(17,300–135,500) (22,000–130,000) (13,600–148,000) ns
Time to HIV infection from enrolment in months (IQR) 9.2 (4.9–14.1) 12.8 (6.6–16.6) 7.4 (3.3–10.6) 0.02
Completed high school % (n) 54.2% (26) 41.7% (10) 66.7% (16) ns
Hormonal contraceptive usea % (n) 97.9% (47) 100% (24) 95.8% (23) ns
Marital Status % (n)
Stable/married partner 79.2% (38) 87.5% (21) 70.8 (17) ns
Single 18.7% (9) 12.5% (3) 25.0% (6) ns
>2 partners 2.1% (1) 0.0% (0) 4.2% (1) ns
Numbers of reported sexual partners in the last 3 months % (n)
0 to 1 93.8% (45) 95.8% (23) 91.7% (22)b ns
2 to 5 6.2% (3) 4.2% (1) 8.3% (2) ns
Reported condom used at last sex act % (n) 68.8% (33) 75.0% (18) 62.5% (15) ns

IQR, interquartile range; PI, post-infection.

Significant values were defined as p < 0.05 and indicated in bold text.

a

Hormonal contraception use included the injectable norethisterone and depomedroxyprogesterone acetate, and oral contraception. One woman in the placebo arm of the study was using an intrauterine device.

b

Two non-rapid progressing women had missing sexual partner data (in previous 3 months) as they refused to answer the question.