EUCTR2009-012141-34-GB
Active, not recruiting
Not Applicable
Randomised Controlled Trial of the Use of Topical Application of Tranexamic Acid in Primary Total Hip Replacement. - (TRANX-H)
niversity Hospital of North Tees and Hartlepool0 sites150 target enrollmentMay 15, 2009
ConditionsBlood loss in total hip replacement in patient with ostoearthritis and rheumatoid arthritis.
DrugsCyklokapron®
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Blood loss in total hip replacement in patient with ostoearthritis and rheumatoid arthritis.
- Sponsor
- niversity Hospital of North Tees and Hartlepool
- Enrollment
- 150
- Status
- Active, not recruiting
- Last Updated
- 14 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\.Undergoing unilateral primary total hip replacement.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1\.2 Adults (18\-64 years) yes
- •F.1\.2\.1 Number of subjects for this age range
- •F.1\.3 Elderly (\>\=65 years) yes
- •F.1\.3\.1 Number of subjects for this age range
Exclusion Criteria
- •1\.Undergoing unilateral primary total hip replacement for tumour.
- •2\.Allergic to Tranexamic acid.
- •3\.Bleeding tendency (e.g. Haemophilic and platelets disorders).
- •4\.Warfarin, treatment dose of LMWH or conventional heparin).
- •5\.History of DVT and pulmonary embolism.
- •6\.Renal failure with creatinine \> 250 micromole/l.
- •7\.Female subjects of child bearing potential must have a negative pregnancy test.
Outcomes
Primary Outcomes
Not specified
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