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Tranexamic acid spray to quickly stop Bleeding in acute Trauma patients

Efficacy of Tranexamic acid spray on reduction of time taken for a complete cessation of Bleeding in acute Trauma patients - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/06/088232
Enrollment
100
Registered
2025-06-04
Start date
Unknown
Completion date
Unknown
Last updated
2025-10-13

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

Conditions

Health Condition 1: T148- Other injury of unspecified body region

Interventions

Intervention1: Tranexamic Acid spray: Tranexamic Acid before bleeding as compared to placebo spray Control Intervention1: Tranexamic Acid (10% w/v): 10% w/v Tranexamic acid spray takes less time than

Sponsors

Shilpa Medicare Ltd.
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adult more than 18 years acute trauma patients with isolated extremity wounds with active bleeding Time since injury - less than 6 hours.

Exclusion criteria

Exclusion criteria: Paediatric trauma patient age less than 18 yrs Patients with known Blood Coagulopathy Patients on anti-platelet and anti-fibrinolytics Patients suffering with Co-morbidities and pregnant women Patients with a history of hypersensitivity to tranexamic acid and any of the ingredients

Design outcomes

Primary

MeasureTime frame
To evaluate the efficacy of Tranexamic acid (TXA) spray 10% w/v with placebo (Placebo spray) on acute injury patients admitted to the ED.Timepoint: Proportion achieving haemostasis within 5, 10, 15 minutes compared to placebo

Secondary

MeasureTime frame
To evaluate the safety of the Tranexamic acid (TXA)spray 10% w/v with placebo (Placebo spray) on acute injury patients admitted to the ED.Timepoint: 1h, 12 h, & 24h post-spray application

Countries

India

Contacts

Public ContactDr Tej Prakash Sinha

AIIMS

Kotarkonda@gmail.com9625109486

Outcome results

None listed

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