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Efficacy of Prophylactic Tranexamic Acid Instillation in Reducing Bleeding Complications During Transbronchial Lung Biopsy: A Randomized Controlled Trial

Prophylaxis Bleeding Complication by instillation Tranexamic acid in Patient with Transbronchial biopsy; A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20241218003
Enrollment
98
Registered
2024-12-18
Start date
2024-04-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

all patients age 18 years or more, diagnosed with abnormal lung mass who required a transbronchial lung biopsy Transbronchial lung biopsy, Bleeding, Tranexamic acid, Adrenaline, Wedge pressure

Interventions

Bronchoscope began with an airway inspection, followed by bronchoalveolar lavage sampling. In tranexamic group, tranexamic acid 50mg/10ml was diluted with normal saline up to 20ml, prepared by the per
Experimental Drug,Placebo Comparator Other
tranexamic acid group,control group

Sponsors

Research of Maharat Nakhonratchasima Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. age at 18 years or more, 2. abnormal lung mass required transbronchial lung biopsy, 3. platelet count equal or greater than 100,000, 4. INR equal or less than 1.2

Exclusion criteria

Exclusion criteria: 1. respiratory failure or impending respiratory failure, 2. unstable hemodynamic status or those receiving inotropic drugs, 3. endobronchial lesion, 4. active hemoptysis, 5. using antiplatelet or anticoagulant therapy within 7 days prior transbronchial lung biopsy, 6. using oral contraceptives or hormonal replacement therapy, 7. pregnancy or breastfeeding, 8. history of bleeding predisposition, 9. venous-thromboembolism, 10. cardiovascular disease, 11. chronic liver disease, 12. chronic kidney disease (GFR < 45 ml/min), 13. urinary tract stones, 14. history of allergy to tranexamic acid

Design outcomes

Primary

MeasureTime frame
Bleeding severity during procedure the Nashville Bleeding Scale

Secondary

MeasureTime frame
interventions to control bleeding during procedure bronchoscopist report,number of biopsy post-procedure bronchoscopist report,procedure duration post-procedure medical record time in and time out,complication up to 2week of follow up patient report, medical record

Countries

Thailand

Contacts

Public ContactSuphanan Autto

Maharat Nakhonratchasima Hospital

s_autto@hotmail.com44235870

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026