Efficacy of Tranexamic Acid in Hemoptysis
Hemoptysis
About this trial
This is an interventional treatment trial for Hemoptysis focused on measuring Hemoptysis, Tranexamic acid, VAS score
Eligibility Criteria
Inclusion Criteria:
- Acute ongoing hemoptysis
- Age: 18 years and above
Exclusion Criteria:
- Pregnant females
- Females on oral contraceptives
- Patients on antifibrinolytics
- Patients with known drug allergy
- Patients with renal failure
- Patients requiring intubation during study period
- Patients with Massive hemoptysis (>600 ml/24 hrs)
Sites / Locations
- Post graduate institute of medical education and research
Arms of the Study
Arm 1
Arm 2
Active Comparator
Placebo Comparator
Tranexamic acid
Placebo
All patients will receive basic resuscitative measures and standard treatment like assessment and management of Airway, breathing, circulation, antitussives, and blood products. Patients in group T will receive Inj Tranexamic acid in a loading dose of 1 g over 10 min followed by an infusion of 1 g over 8 h.
All patients will receive basic resuscitative measures and standard treatment like assessment and management of Airway, breathing, circulation, antitussives, and blood products. Patients will receive 0.9% normal saline instead of Tranexamic acid.