Salpingitis Shuanghuanglian injection clinical study of obstructive_0.doc

Salpingitis Shuanghuanglian injection clinical study of obstructive_0.doc

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Salpingitis Shuanghuanglian injection clinical study of obstructive_0

 PAGE \* MERGEFORMAT 24 Salpingitis Shuanghuanglian injection clinical study of obstructive Of: Xu Huijun, Zhang, Gu Jin-Hong, Lin Jing [Abstract] Objective To investigate the injection side of the dome closed Shuanghuanglian Salpingitis treatment efficacy and mechanism of obstruction. Methods 200 patients of 386 fallopian tubes for the study. By randomized block divided into treatment group and three control groups, observation group (Shuanghuanglian injection side of the dome injection), control group 1 (lincomycin injection side of the dome injection group), control group 2 (tubal surgery group) and control group 3 (tubal Dilation group) 50 cases. observed 4 cases of blocked fallopian tubes before and after treatment to improve the situation, and blood rheology and interleukin -2 and immunoglobulin IgA, IgG, IgM changes. Shuanghuanglian injection side of the dome of the results of treatment of the total closed efficiency of 97.96%, Shuanghuanglian injection in patients with blood stasis condition has improved, hyperviscosity, enhance immune function. Conclusion Shuanghuanglian injection side of the dome closed treatment of salpingitis obstruction has a good clinical effect, its efficacy patients through the correct state of Noxious Heat stasis, improve pelvic microcirculation, improve immune function and achieve. [Keywords:] Shuanghuanglian injection, salpingitis obstruction, the side dome closed, hemorheology, interleukin -2, immunoglobulin Abstract: Objective To investigate the effect of Shuanghuanglian injection parafornix-injecting in treating uterine tube obstruct (UTO) and explore its mechanism. Methods Clinic study included 386 uterine tubes of 200 patients, which were randomly divided into treatment group (50 cases, treated with Shuanghuanglian injection parafornix-injecting) and three control groups - group one (50 cases, treated with Lincocin vial parafornix-injecting), group two (50 cases, treated with hydrotubation) and group three (5

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