Successful ventricular arrhythmia (VA) ablation requires identification of functionally critical sites during contact mapping. Estimation of the peak frequency (PF) component of the EGM may improve correct near field (NF) annotation to identify circuit segments on the mapped surface. In turn, assessment of near- and far field (FF) EGMs may delineate the 3-dimensional path of a VT circuit. A proprietary NF detection algorithm was applied retrospectively to scar-related re-entry VT maps and compared to manually reviewed maps employing first deflection (FDcorr) for VT activation maps and last deflection (LD) for substrate maps. VT isthmus location and characteristics mapped with FDcorr vs. NF were compared. Omnipolar low voltage areas, late activating areas and deceleration zones in LD vs NF substrate maps were compared. On substrate maps, PF estimation was compared between isthmus and bystander-sites. Activation mapping with entrainment and/or VT termination with RF ablation confirmed critical sites. 18 patients with high-density VT activation and substrate maps (55.6% ischemic) were included. NF detection correctly located critical parts of the circuit in 77.7% of the cases compared to manually reviewed VT maps as reference. In substrate maps NF detection identified deceleration zones in 88.8% of cases which overlapped with FDcorr VT isthmus in 72.2% compared to 83.3% overlap of DZ assessed by LD. Applied to substrate maps, PF as a stand-alone feature did not differentiate VT isthmus-sites from low voltage bystander-sites. Omnipolar voltage was significantly higher at isthmus-sites with longer EGM durations compared to low voltage bystander-sites. The NF algorithm may enable rapid high-density activation mapping of VT circuits in the near field of the mapped surface. Integrated assessment and combined analysis of near and far field EGMs could support characterisation of 3-dimensional VT circuits with intramural segments. For scar-related substrate mapping, PF as a stand-alone EGM feature did not enable the differentiation of functionally critical sites of the dominant VT from low voltage bystander sites in this cohort.