Background: Early detection of extended-Spectrum β,-lactamases (ESBLs) producing bacteria is critical for infection prevention and control. Numerous phenotypic approaches and automated systems have been developed for detecting ESBL bacteria. However, there is a scarcity of data in Ethiopia regarding the most reliable, simple, and cost-effective Methods for detecting ESBL-producing bacteria. This study, therefore, aimed to evaluate the diagnostic performance of three phenotypic approaches for detecting ESBL-producing bacteria. Methods: In this study, 117 isolates of Klebsiella pneumoniae, Escherichia coli, Klebsiella oxytoca, and Proteus mirabilis were examined. Cefotaxime (30 μ, g) and ceftazidime (30 μ, g) were used for screening ESBL enzymes. A screening breakpoints of ≤,27 mm and ≤,22 mm were used for cefotaxime (30 μ, g) and ceftazidime (30 μ, g), respectively, as per the Clinical and Laboratory Standards Institute (CLSI) guidelines. All 117 strains were further confirmed by the Vitek 2 compact, double disk synergy, ESBL Epsilometer test, and combined disk Method. The combined disk Method was adopted as the reference Method. Results: Out of 117 isolates, 90 (86%) had zone diameters of ≤,27 mm and ≤,22 mm for cefotaxime (30 μ, g) and ceftazidime (30 μ, g), respectively. The reference Method detected 76 (65%) ESBL isolates out of 117 ones. From among the three techniques (i. e., double disk synergy, Vitek 2 compact, and ESBL Epsilometer test), the double disk synergy Method demonstrated overall sensitivity and specificity of 97. 4% and 97. 6%, respectively. Vitek-2, cefotaxime, and ceftazidime Epsilometer test indicated indeterminate results of 6. 8%, 6. 8%, and 5. 1% respectively. Conclusion: Double disk synergy was found to have the highest sensitivity and specificity for detecting ESBL isolates with no indeterminate results.