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. 2008 Oct;4(5):843–853. doi: 10.2147/tcrm.s3426

Table 2.

Summary of reported microbiologic and clinical efficacy data

Condition Efficacy after completion of therapy
No. subjects evaluated Days post-therapy Significantly different from comparator(s)?a
Microbiologic Clinical
Klimberg et al 1998c cUTI 95.3% 93.0% 171 5–9 Nof
Peng 1999d AP and cUTI 90.0% 90.0% 20 −5 No
Peterson et al 2008b AP and cUTI 79.8% 82.6% 317 5–7 No
Richard et al 1998ac,e AP 94.0% 92.0% 89 5–9 Nog
Richard et al 1998b cUTI 91.0% 92.0% 126 5–9 No
a

alpha = 0.05.

b

Data are presented from the modified intention to treat analysis.

c

Data are presented from the microbiologically evaluable study subjects; efficacy not reported for intention to treat or modified intention to treat groups.

d

No end of therapy endpoint assessed. Data presented was collected on day 5 of therapy.

e

Publication reports the findings of two trials; average efficacy presented here.

f

Statistical comparison performed only for microbiologic efficacy outcome.

g

No statistical comparisons reported; however, microbiologic and clinical efficacy rates for levofloxacin were higher than for the comparators.

Abbreviations: AP, acute pyelonephritis; cUTI, complicated urinary tract infection.