Objects: To evaluate safety and efficacy of vaginal misoprostol alone with vaginal misoprstol for cervical ripining followed by suction and evacuation method Method : A prospective randomized study was done over a period of 5 years including 100 patients. In group - I misoprostol GOOjugm vaginal was followed by 200agm every 3 hours till abortion occurred. In group II, 600ugm of vaginal misoprostol used for repining of cervix followed by suction and evacuation after 6 hrs. Results : Induction abortion interval was significantly lower in Group - II 6.26±6.08 hours than group I 15.78 ± 9.02 hours.