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Effects of oral tranexamic acid in patient with CRSwNP undergoing FESS

Effects of oral tranexamic acid on intra-operative blood loss and surgical field quality during endoscopic sinus surgery in patients with Chronic rhinosinusitis with nasal polyps

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20250707011
Enrollment
20
Registered
2025-07-07
Start date
2025-06-24
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

Intra-operative blood loss during Endoscopic sinus surgery in patient with Chronic Rhinosinusitis with Nasal Polyp Oral Tranexamic Acid, TXA, Oral TXA, CRSwNP, Chronic rhinosinusitis with Nasal Polyp, Endoscopic Sinus Surgery, ESS

Interventions

Placebo 2 tabs po q 6 hr for 4 doses,Oral Tranexamic Acid (500 mg) 2 tabs po q 6 hr for 4 doses
Placebo,Oral Tranexamic Acid

Sponsors

None
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients aged 18 to 65 years who receive treatment at the Otolaryngology outpatient department, Department of Otolaryngology, Phramongkutklao Hospital. 2. Patients who consent to participate in the research study. 3. Patients diagnosed with chronic rhinosinusitis with nasal polyps. 4. Patients who are scheduled to undergo functional endoscopic sinus surgery. 5. Patients with ASA physical status class 1 or 2.

Exclusion criteria

Exclusion criteria: 1. Patients younger than 18 years. 2. Patients who do not consent to participate in the research study. 3. Patients with ASA physical status class 3 or higher. 4. Patients with a history of thromboembolic disease. 5. Patients with a history of allergic reactions or contraindications to tranexamic acid. 6. Patients with abnormal liver function or a history of liver disease with AST/ALT more than 3 times the upper normal limit. 7. Patients with kidney disease or a history of chronic kidney disease with ESRD or eGFR < 30. 8. Patients with blood disorders or on anticoagulants or antiplatelet medications that cannot be discontinued prior to surgery. 9. Patients with other conditions that may increase the risk of bleeding complications.

Design outcomes

Primary

MeasureTime frame
Bood loss Intra-operative Millilitres

Secondary

MeasureTime frame
Surgical field quality Intra-operative Boezaart surgical field grading scale

Countries

Thailand

Contacts

Public ContactThanit Chalermwattanachai

Doctor

ninontkt@gmail.com0819952415

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026