Tendinopathy includes cases with chronic tendon pain and spontaneous tendon ruptures, which is putatively resulted from failed tendon healing. Overuse is a major risk factor of tendinopathy, which can impose mechanical and oxidative stress to tendons. Previous studies investigated the influences of mechanical stress, but the direct impact of oxidative stress on tendon healing remains unclear. We hypothesized that imposed oxidative stress can impair tendon healing and lead to tendinopathic changes. Thirty-nine rats were operated for patellar tendon window injury. From week 3 to 5 post operation, the rats receive three weekly subcutaneous injections of saline, 50µM or 500µM H2O2 (n=13) over patellar tendon. Gait analysis for pain assessment and 3D ultrasound imaging for detection of tendinopathic changes were performed at pre-injury and 6 weeks post operation. At week 6, knee specimens were harvested for histology or tensile mechanical test. Elastic modulus of the healing patellar tendons was significantly lower in 50µM but not 500µM H2O2 group, while ultimate mechanical stress was not significantly different across groups. Similarly, only the 50µM H2O2 group exhibited pain-associated gait asymmetry. Significant tendon swelling with increased tendon volume was observed in the 50µM H2O2 group. There were hypoechogenic changes in the tendon wound, but there was no significant difference in percentage vascularity. H2O2 impaired tendon healing and elicited tendinopathic changes, with respect to pain and structural abnormalities. Oxidative stress plays a role in the failed tendon healing of tendinopathies, and H2O2-induced failed tendon healing may serve as a good animal model to study tendinopathy.