Methods: This is a descriptive study that was conducted in 2019-2021. The statistical population consisted of 160 patients who were candidates for termination of pregnancy and were divided into two groups of 80 people, one group with misoprostol 50 micrograms which was administered as an oral solution up to a maximum dose of 200 micrograms and the other group with oxytocin ampoules with Initial doses of 10 units were induced. The success rate in each group was considered to achieve appropriate contractions (three contractions in ten minutes, each lasting 40 seconds) and finally the rate of successful normal delivery. The collected data were analyzed using Mann-Whitney, Chi-square and t-test.