Extrusion is one of the most common methods of twisting chemical thread [l]. The moving thread is exposed to forces directed along and perpendicular to its axis and it heats up as a result.Two stages can be distinguished in the deformation that takes place in extrusion of the thread [2,3]. Stresses for which failure and disorientation of the structure of the polymer begin arise in the fibres in the first stage under the effect of longitudinal and radial compression and heat, and the cross section of the fibres increases slightly. The second stage is characterized by loss of stability of the structure and the appearance of kinks in the fibre, and further failure of the polymer up to total disorientation takes place at the kinking points.Since the thread-twisting time is very brief in practice, we can hypothesize that only elastic strains occur. Highly elastic and plastic strains and all structural changes responsible for fixing crimps are realized later, when the thermofixed crimped thread moves into the chamber.During fabrication of polycaproamide (PCA) textured twist thread, complex changes take place in the fibre which are highly dependent on the principle of attaining the texturing effect, and this is determined by the model of the machine and the process regime used.The texturing process is complicated and specific. At the Vidin Polyamide Fibre Plant, PCA textured twists for carpets are fabricated on Textima 1023 machines which operate on the Bancroft method. The results of a study of the structural changes that take place during fabrication of Vidlon PCA twists on these machines are reported here.Assuming that the data from x-ray structural analysis of textured thread cannot in principle be used for evaluating their structural differences, we conducted our studies in a slightly different direction. The crystallinity of the polymer was indirectly judged with the results of differential scanning calorimetry (DSC). The molecular orientation was characterized with the birefringence (An) found with an Ampliwalpole D polarizing microscope. The density of the fibres was determined by the gradient tube method using immersion fluid.The structural differences in fibres can be judged by their behavior in dyeing. Based on this opinion we conducted tests using a monosulfonic acid dye "'Nilosan Blue PRL" in a concentration of 1% of the weight of the fibres, at a temperature of 60~ and pH = 5. Before dyeing, the samples were treated with an aqueous solution containing 2 g/liter of Diadawin EWN (20%) and 3 g/liter of Na3PO 4, then washed and dried at room temperature. The anaount of absorbed dye was determined by the extinction of the residual dye bath using a Spekol-10 spectrophotometer.