Clinical Observation Of The Effect Of Cervical Softening No.1 On The Cervical Ripening Of The First Parturients Of Full-term Pregnancy

Objective: Through the use of cervical softening No.1 for pregnant women with full-term pregnancy with blood stasis syndrome,the effect of cervical softening No.1 on promoting cervical ripening in pregnant women with full-term pregnancy was preliminarily investigated.Methods:A total of 160 unproduced primiparas who met the inclusion criteria were randomized into the observation group(cervical softening group 1)and the control group(placebo group),with 80 patients in each group.The cervical maturity score(Bishop score),the outcome of the delivery,and the effect on the maternal fetus were observed before and after treatment.Results:Cervical scores of pregnant women in the experimental group were significantly higher than those in the control group(P<0.05),and the cervical ripening effect of the experimental group was significantly better than that of the control group(P<0.01).The vaginal delivery rate of the experimental group was higher than that of the control group after treatment,and the difference was statistically significant(P<0.05).There were no significant differences in adverse events,neonatal birth,and postpartum hemorrhage between the two groups(P>0.05).Conclusion:Cervical softening No.1 can promote cervical ripening safely and effectively,with mild effect,no obvious adverse effects on mother and child,and play an active role in reducing cesarean section rate and promoting natural childbirth.