Adults 18 to 90, any sex, with Musculoskeletal Cancer or Sarcoma,Soft Tissue. Patients with the condition only — healthy volunteers not accepted.
Results — posted to ClinicalTrials.gov
Per-arm endpoint measurements with 95% confidence intervals where reported. Source: trial results section.
Perioperative Blood LossPrimary· During surgical procedure, 4 to 6 hours
How much blood was lost during surgical process
Group
Value
95% CI
Bony Tumor no TXA Group
283
250 – 350
Soft Tissue Tumor w/ TXA Group
700
100 – 1800
Soft Tissue Tumor With no TXA Group
416
100 – 700
Sponsor's own description
This study intends to determine if any correlation exists between administration of TXA or not to musculoskeletal oncology patients undergoing endoprosthetic reconstruction and blood loss and blood transfusion rates.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
NCT07332910 — Study the Anti-inflammatory Effect of Tranexamic Acid When Used in Anterior Cruciate Ligament Reconstruction.
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· active not recruiting
NCT07212452 — Tranexamic Acid : Nebulization vs IV Route for Hemoptysis
· Phase 2, PHASE3
· completed
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Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
Sponsor: as reported to ClinicalTrials.gov by University of Kansas Medical Center
Last refreshed: 21 May 2025
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04347122.