Aim:The aim of this study is to investigate the effect of pentoxifylline (PTX) and milrinone on the stasis zone in rats for which an experimental burn model was established. Method: In this study with an experimental design, PTX and milrinone -5-phosphodiesterase inhibitors -were administered orally and intraperitoneally to rats for which an experimental burn model was created. The effects of these pharmacological agents on the stasis zone and comparison of these effects with each other were investigated. In the study, 56 4-monthold female rats of Wistar albino type with a weight of 200 ± 10% g were used. The rats were divided into seven groups. The burn model defined by Regas and Erlich was applied to 48 rats under anesthesia. Groups 1, 2, and 3 were defined as the sham group, intraperitoneal control group, and oral control group, respectively. Drugs were administered to groups for 10 days as follows: PTX intraperitoneally daily at a dose of 50 mg/kg to Group 4, PTX orally daily at a dose of 50 mg/kg to Group 5, milrinone intraperitoneally daily at a dose of 1 mg/kg to Group 6, and milrinone orally daily at a dose of 1 mg/kg to Group 7. All rats were sacrificed on the 10 th day of the experiment. Serum samples for the biochemical levels of malondialdehyde (MDA), glutathione peroxidase (GPx), superoxide dismutase (SOD), and catalase were taken as well as tissue samples for the histopathological study of these. Results: Pathologically, edema, hyperemia, epithelial degeneration, necrosis, inflammatory filtration, and fibrosis measurements were taken. Compared to the control group, the tissue damage score was lower in all treated groups. MDA levels were lower in the intraperitoneal and oral PTX administered group than in the control group, while SOD, catalase, and GPx levels were higher. MDA levels were lower in the intraperitoneal and oral milrinoneadministered group than in the control group, and SOD, catalase, and GPx levels were higher. In addition, it was found that MDA levels were lower and SOD, catalase, and GPx levels were higher in the intraperitoneal PTX-administered group than in the intraperitoneal milrinone-administered group. It was found that MDA levels were lower and SOD, catalase, and GPx levels were higher in the oral PTX-administered group than in the oral milrinone-administered group. Conclusion: As a result of our study, it was shown that PTX and milrinone reduce oxidative stress and have positive effects, improving wound healing in the burn model established for the rats.