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The Role of Inhalations of Tranexamic Acid in Patients With Hemoptysis

Status
UNKNOWN
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01496196
Enrollment
100
Registered
2011-12-21
Start date
2012-01-31
Completion date
2016-02-29
Last updated
2015-04-14

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

Conditions

Hemoptisis

Keywords

hemoptisis, bleeding, tranexamic acid

Brief summary

Hemoptysis is defined as the expectoration of blood from respiratory tract, a spectrum that varies from blood-streaking of sputum to coughing up large amounts of pure blood. Massive hemoptysis variably defined as the expectoration of 100-600 ml over 24-h period. The most common site of bleeding is the tracheobronchial tree, which can be affected by inflammation (acute or chronic bronchitis, bronchiectasis) or by neoplasm ( bronchogenic carcinoma, endobronchial metastatic carcinoma, bronchial carcinoid tumor). The bronchial arteries, which originate either from aorta or from intercostal arteries, and are part of the high-pressure systemic circulation, are the source of bleeding in bronchitis or bronchiectasis or endo bronchial tumors.

Interventions

DRUGtranexamic acid

500 mg/5 ml 3-4 times a day

Sponsors

Meir Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* Age \> 18 * Hemodynamicaly stable * Hemoptysis of varying etiologies * Coumadin treatment will be switched to clexane or heparine

Exclusion criteria

* Age \< 18 * Hemodinamicaly unstable * Massive hemoptysis ( \> 200 ml / day) * Renal failure: creatinine \> 3, renal replacement treatment * Hepatic failure: bilirubin \> 2 mg/dl, AST \> 3 of upper normal limit level * Coagulation disorders, INR\> 2. * Hypesensitivity to tranexamic acid * Pregnant woman

Design outcomes

Primary

MeasureTime frame
bleeding stops1 year

Countries

Israel

Contacts

Primary ContactDavid Shitrit, Dr.
Davids3@clalit.org.il09-7471556

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 5, 2026