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Comparing the effectiveness of prophylactic infusion of intravenous tranexamic acid with placebo during flexible bronchoscopy

Comparing the effectiveness of prophylactic infusion of intravenous tranexamic acid with placebo in non-life-threatening bleeding during flexible bronchoscopy

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230204057318N6
Enrollment
60
Registered
2024-10-19
Start date
2024-10-25
Completion date
Unknown
Last updated
2025-01-08

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

Conditions

Bronchoscopy for all reasons. Other diseases of bronchus, not elsewhere classified

Interventions

Intervention 1: Intervention group: Infusion of 10 mg/kg tranexamic acid in 50mL normal saline will administered 20 minutes before the procedure begins. Intervention 2: Control group: Placebo (normal

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Candidate for elective or emergency flexible bronchoscopy and biopsy (TBLB) Mental health and providing informed consent

Exclusion criteria

Exclusion criteria: Anticoagulant agent consumption Having a known blood Abnormality or coagulopathy Chronic liver disease Chronic kidney disease with a serum creatinine level of more than 2 mg/dL History of seizures Sensitive to antifibrinolytics

Design outcomes

Primary

MeasureTime frame
Hemorrhage during the procedure. Timepoint: Intraoperative. Method of measurement: Suction volume.

Secondary

MeasureTime frame
The amount of local epinephrine or cold saline needed to control bleeding. Timepoint: Intraoperative. Method of measurement: Volume of used fluid.;Duration of operation. Timepoint: intraoperative. Method of measurement: Minune.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAlireza Shakeri

Shahid Beheshti University of Medical Sciences

dr.alirezashakeri@gmail.com+98 21 7343 0000

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026