Karabay 2004.
Methods | Randomized controlled trial Duration: December 1999 and December 2001 |
|
Participants | Number: 34 patients enrolled Inclusion criteria: the presence of signs and symptoms compatible with brucellosis including a positive agglutination titre (≥1/160) and/or a positive culture. Exclusion criteria: history of seizure, pregnancy, and age under 15 years. |
|
Interventions | 1‐doxycycline 100 mg two times daily and rifampicin 600 mg once daily for 45 days 2‐ofloxacin 400 mg once daily and rifampicin 600 mg once daily for 30 days |
|
Outcomes | 1‐clinical relapse 2‐adverse drug reactions 3‐time to defervescence |
|
Notes | Location: the Social Security Duzce Hospitaland Abant Izzet Baysal University, Duzce Medical School, Turkey. Setting: hospitalised patients Source of funding: not mentioned |
|
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Not described |
Allocation concealment (selection bias) | Unclear risk | Not described |
Blinding (performance bias and detection bias) All outcomes | High risk | Open study |
Incomplete outcome data (attrition bias) All outcomes | High risk | 18 patients were randomized to DR, and 16 to OR. Four patients in DR and 1 in OR did not appear in follow‐ups. Four left because they felt well, and one refused to use the drugs. However, the proportion of missing outcomes compared with observed events was considerable. |
Selective reporting (reporting bias) | Low risk | Important outcomes are reported |
Other bias | Low risk |