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贞芪补血口服液联合孕激素治疗气血肾虚型月经后期、月经过少随机对照试验

Effectiveness of Zhenqi Buxue Oral Liquid Combined with Progesterone for Treatment of Oligomenorrhea and Hypomenorrhea with Qi-Blood and Kidney (Shen) Essence Deficiency: A Randomized Controlled Trial.

机构信息

National Clinical Research Center for Obstetric & Gynecologic Diseases, Department of Obstetrics and Gynecology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College Address: Peking Union Medical College Hospital (East), Beijing, 100730, China.

Department of Obstetrics and Gynecology, Liuzhou Maternal and Child Health Care Hospital, Liuzhou, Guangxi Zhuang Autonomous Region, 545001, China.

出版信息

Chin J Integr Med. 2023 Nov;29(11):963-970. doi: 10.1007/s11655-023-3740-y. Epub 2023 Aug 18.

Abstract

OBJECTIVE

To evaluate the effectiveness and safety of Zhenqi Buxue Oral Liquid (ZQ), progesterone capsules, and their combination in treating oligomenorrhea and hypomenorrhea with qi-blood and Kidney (Shen) essence deficiency.

METHODS

This was a prospective, randomized, multi-center controlled trial between June 2022 to December 2022. Ninety-six oligomenorrhea and hypomenorrhea patients with qi-blood and Shen essence deficiency were randomly assigned to receive ZQ (ZQ group, 29 cases), progesterone capsules (PG group, 32 cases), or the combined Chinese and Western medicine (COM group, 31 cases) at a ratio of 1:1:1. Patients in the ZQ or PG group took daily 10 mL twice a day of ZQ or 200 mg once a day of progesterone capsules for 10 consecutive days on day 15 of the menstrual cycle respectively, and patients in the COM group received the same ZQ combined with progesterone capsules. The treatment course lasted for 3 months and follow-up was performed at 1 and 3 months after the end of treatment. Primary endpoint was the menstrual Traditional Chinese Medicine Syndrome Scale (TCMSS) scores. Secondary endpoints included pictorial blood loss assessment chart (PBAC) scores, clinical efficacy rate, 36-item Short Form Health Survey (SF-36) scores, sex hormones and thickness of endometrium. Adverse events (AEs) were recorded.

RESULTS

TCMSS scores after 1- and 3-month treatment in all groups were significantly lower than those at baseline (P<0.05). Only TCMSS scores after 3-month treatment in the ZQ and COM groups continuously decreased compared with those after 1-month treatment in the same group (P<0.01). TCMSS scores after 3-month treatment in the ZQ and COM groups were significantly lower than those in the PG group (P<0.05, P<0.01). Compared with baseline, PBAC scores in the ZQ and COM groups after 3 months of treatment were also significantly higher (both P<0.01). The total effective rates of TCM syndrome of 3-month treatment were significantly improved in all groups compared with that after 1 month of treatment (P<0.05). The total effective rate of the COM group was the highest in the 3rd month of treatment and significantly higher than that of PG group alone (P<0.05). Compared with baseline, only the SF-36 scores of COM group were significantly improved after 3 months of treatment (P<0.05). No serious adverse reactions were observed after treatment.

CONCLUSIONS

The combination of ZQ and PG, or ZQ only had better effects on reducing TCMSS scores compared with PG, and COM showed the higher total effective rate compared with monotherapy. Besides, COM could effectively improve menstrual blood loss and quality of life. ZQ combined with PG may be an effective and safe option for oligomenorrhea and hypomenorrhea patients with qi-blood and Shen essence deficiency.

摘要

目的

评价贞芪补血口服液、黄体酮胶囊及其联合治疗气血肾虚型月经过少、月经后期的有效性和安全性。

方法

这是一项前瞻性、随机、多中心对照试验,于 2022 年 6 月至 2022 年 12 月进行。96 例气血肾虚型月经过少、月经后期患者随机分为贞芪补血口服液组(ZQ 组,29 例)、黄体酮胶囊组(PG 组,32 例)和中西药联合组(COM 组,31 例),比例为 1:1:1。ZQ 组或 PG 组患者在月经周期第 15 天分别每日口服 10 mL,每日 2 次,或每日口服 200 mg,共 10 天。COM 组患者同时服用相同剂量的贞芪补血口服液和黄体酮胶囊。治疗疗程为 3 个月,治疗结束后 1 个月和 3 个月进行随访。主要终点为中医证候量表(TCMSS)评分。次要终点包括图片出血量评估表(PBAC)评分、临床有效率、36 项简明健康状况量表(SF-36)评分、性激素和子宫内膜厚度。记录不良事件(AE)。

结果

治疗 1 个月和 3 个月后,所有组的 TCMSS 评分均明显低于基线(P<0.05)。仅 ZQ 组和 COM 组治疗 3 个月后的 TCMSS 评分较同组治疗 1 个月后持续下降(均 P<0.01)。治疗 3 个月后,ZQ 组和 COM 组的 TCMSS 评分明显低于 PG 组(P<0.05,P<0.01)。与基线相比,ZQ 组和 COM 组治疗 3 个月后的 PBAC 评分也明显升高(均 P<0.01)。与治疗 1 个月相比,所有组治疗 3 个月后的中医证候总有效率均明显提高(均 P<0.05)。COM 组治疗 3 个月后的总有效率最高,明显高于单独 PG 组(P<0.05)。与基线相比,只有 COM 组治疗 3 个月后的 SF-36 评分明显改善(P<0.05)。治疗后未观察到严重不良反应。

结论

与 PG 相比,ZQ 联合 PG 或单独使用 ZQ 对降低 TCMSS 评分的效果更好,COM 显示出比单药治疗更高的总有效率。此外,COM 可有效改善月经失血和生活质量。ZQ 联合 PG 可能是气血肾虚型月经过少、月经后期患者的一种有效、安全的选择。

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