Puerariae Decoction For Primary Dysmenorrhea Of Cold-damp Stagnation Type On Clinical Observation

Objective:As a summary of the research progress of Primary dysmenorrhea,by comparing clinical pain VAS score,serum PGF2?,TCM syndrome score,to evaluate the effectiveness and safety of Puerariae Decoction and Lesser Abdomen Stasis-Eepellmg Decoction in the treatment of primary dysmenorrhea of cold damp stagnation,to provide reference for its clinical application.Methods:(1)96 cases according to the criteria of cold damp stagnation type in patients with primary dysmenorrhea were randomly divided into Puerariae Decoction group,Lesser Abdomen Stasis-Eepellmg Decoction group,and placebo group,each group include 30 cases.(2)The Primary dysmenorrhea group was given Primary dysmenorrhea orally,the Lesser Abdomen Stasis-Eepellmg Decoction given Lesser Abdomen Stasis-Eepellmg Decoction,the placebo group was given placebo decoction,in 7 days before the menstrual,and even served 7 agent,continuous treatment of 3 menstrual cycles for a course of treatment.(3)By comparing clinical pain VAS score,serum PGF2?,TCM syndrome score,to evaluate the effectiveness and safety of Puerariae Decoction.(4)Us SPSS18.0 to carry on the statistically analysis,compare and determine the clinical curative effect and safety through the treatment before and after in the same group and in the different groups.Results:(1)General information and baseline condition,the difference between the three groups was not statistically significant(P>0.05),equallycomparable pressure.(2)The disease curative effect of three groups of patients,Puerariae Decoction group total effective rate was 96.67%,the clinical cure in 40%;the lower abdomen Lesser Abdomen Stasis-Eepellmg Decoction group total effective rate was 93.33%,the clinical cure in26.67% patients in the placebo group;the total effective rate was 23.33%,the recent clinical cure 0.00%.Puerariae Decoction group and Lesser Abdomen Stasis-Eepellmg Decoction group compared with placebo group,the differences were statistically significant(P<0.05);Puerariae Decoction group and Lesser Abdomen Stasis-Eepellmg Decoction group,the difference was not statistically significant(P>0.05).The results showed that Puerariae Decoction group and Lesser Abdomen Stasis-Eepellmg Decoction group can effectively improve the cold damp stagnation type primary dysmenorrhea.(3)From the symptom curative effect of three groups of patients,Puerariae Decoction group total effective rate was 96.67%,the clinical cure in 50%;the lower abdomen Lesser Abdomen Stasis-Eepellmg Decoction group total effective rate was 93.33%,the clinical cure in 26.67% patients in the placebo group;the total effective rate was 33.33%,the recent clinical cure 0.00%.Puerariae decoction group and Lesser Abdomen Stasis-Eepellmg Decoction group compared with placebo group,the differences were statistically significant(P<0.05),Puerariae Decoction group and Lesser Abdomen Stasis-Eepellmg Decoction group,the difference was statistically significant(P<0.05),description of Puerariae Decoction group and Lesser Abdomen Stasis-Eepellmg decoction can effectively improve the differences between the three groups of cold damp stagnation type primary Dysmenorrhea syndrome,Puerariae Decoction group in the improvement of primary dysmenorrhea of cold damp stagnation syndrome than Lesser Abdomen Stasis-Eepellmg Decoction group.(4)With the treatment of drug related adverse reactions were not found in any of the three groups were safe and reliable.Conclusion: Puerariae Decoction and Lesser Abdomen Stasis-Eepellmg Decoction in the treatment of cold damp stagnation type primary dysmenorrhea is safe and effective,and the curative effect of Puerariae Decoction syndrome curative effect the total effective rate and total effective rate were higher than the Lesser Abdomen Stasis-Eepellmg Decoction group.