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临床试验/NCT06707051
NCT06707051已完成2 期

Comparison of Efficacy of Tranexamic Acid and Calcium Dobesilate for Bleeding of Endometrial Origin

District Headquarters Teaching Hospital Sahiwal1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2022年1月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
100
试验地点
1
主要终点
Reduction in blood loss

研究概览

简要总结

Abnormal uterine bleeding is characterized by excessive menstrual blood loss affecting over 50% of women of reproductive age. It can be debilitating and significantly affect a woman's quality of life. Tranexamic acid (TXA) prevents the breakdown of clots and fibrinolysis by binding to the lysine receptor on plasminogen while Calcium dobesilate improves microcirculation and vascular health by increasing nitric oxide synthesis leading to endothelium relaxation, so inhibits endothelial shedding. Calcium dobesilate and tranexamic acid have roles in managing bleeding disorders, but their use and efficacy can vary. Tranexamic acid is more established and widely used for abnormal bleeding, while calcium dobesilate role is less defined and more variable. Tranexamic acid reduces menstrual blood loss, but it has no affect on endothelium while calcium dobesilate reduces the oxidative stress , so improving endothelial health and provide the endothelial protection. Side effects include GI upset , hypersensitivity reactions and agranulocytosis. The side effects of both drugs are comparable.

详细描述

This Randomized control trial was conducted at Obstetrics & Gynaecology unit Sahiwal Teaching Hospital from to for the period of two years after taking the approval from Institutional review board (IRB). Sample size of one hundred patients (Fifty in each group) was calculated. These patients were randomly allocated into two equal groups, fifty patients in each group. Written informed consent was obtained from each subject by explaining the risks and benefits associated with the drugs. Group A women were given 500mg tranexamic acid thrice a day for 5 days during menstrual cycle and in group B women were given 500 mg capsule Calcium dobesilate thrice a day for 5 days during menstruation for consecutive time period of three months. Women were also evaluated for adverse effects. The information was entered into specially designed proformas. The data was analyzed by SPSS version 21.0. Frequencies and percentages of categorical variables including marital status, parity and adverse effects were calculated and compared between two groups by applying chi square tests. t-Test was used for the calculation of mean and standard deviations of numerical variables like age, BMI, duration of symptoms, blood loss before and after intervention and reduction in blood loss and was compared between two groups. In all statistical analysis only p value less than 0.05 was considered significant.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 40 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Women of 18-40 years
  • Abnormal uterine bleeding

排除标准

  • Patients with pregnancy
  • Miscarriage
  • Hypersensitivity to pharmacological agents to be used in trial
  • Patients having moderate to severe anemia (Hb:<8gm/dl)
  • Patients with thyroid abnormalities (TSH > 5mIU)
  • Benign uterine conditions e.g. fibroid uterus, endometrial/cervical polyp
  • Uterine malignancy
  • Coagulation disorders (PT : >15sec).

研究组 & 干预措施

Group A

Experimental

Group A included 50 Patients fulfilling the inclusion and exclusion criteria, was given Tranexamic acid for bleeding of endometrial origin

干预措施: Tranexamic Acid (Drug)

Group B

Experimental

Group B included 50 Patients fulfilling the inclusion and exclusion criteria, was given Calcium Dobesilate for bleeding of endometrial origin

干预措施: Calcium dobesilate (Doxium) (Drug)

结局指标

主要结局

Reduction in blood loss

时间窗: Three months

Blood loss at baseline and three months after treatment will measured. Reduction in blood loss will be calculated after three months of treatment

次要结局

未报告次要终点

研究者

发起方
District Headquarters Teaching Hospital Sahiwal
申办方类型
Other
责任方
Principal Investigator
主要研究者

Mahpara Shaukat

associate professor

District Headquarters Teaching Hospital Sahiwal

研究点 (1)

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