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Effect of Tranexamic Acid and Calcium Dobesilate for Bleeding of Endometrial Origin

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

Status
Completed
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06707051
Acronym
TXA
Enrollment
100
Registered
2024-11-27
Start date
2022-01-01
Completion date
2024-06-30
Last updated
2024-11-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Abormal utèrine Bleeding, Agranulocytosis, Bleeding, Bleeding Pattern, Endometrial, Endometrial Bleeding, GI Disturbance, Heavy. Mentrual Bleeding, Hypersensitivity Response, Uterine Bleeding

Keywords

Tranexamic acid, Calcium Dobesilate, Bleeding of endometrial origin, TXA

Brief summary

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.

Detailed description

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.

Interventions

DRUGTranexamic Acid

Group A received Trannexamic Acid 500mg three times a day for 5 days

Group B recieved Cap.Calcium Dobesilate 500mg 3 times a day for 5 days

Sponsors

District Headquarters Teaching Hospital Sahiwal
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

* Women of 18-40 years * Abnormal uterine bleeding

Exclusion criteria

* 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).

Design outcomes

Primary

MeasureTime frameDescription
Reduction in blood lossThree monthsBlood loss at baseline and three months after treatment will measured. Reduction in blood loss will be calculated after three months of treatment

Countries

Pakistan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026