Comparison of the Efficacy of Ultrasound-guided Supra-inguinal Fascia Iliaca and Lumbar Erector Spina Plan Block in Hip Fractures
NCT07639762
Agnosia, Femoral Fractures
Istanbul, Sancaktepe, Turkey (Türkiye)
View Trial DetailsNCT Number: NCT02736383
To determine if TXA utilization is effective at reducing transfusion rates in elderly patients undergoing surgery for treatment of a hip fractures.
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Notify Me65 year and older
All sexes
Observational
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: 6 weeks
Blood transfusion rates during the patients hospital stay will be assessed.
Time frame: 6 weeks
The patients length of stay in the hospital will be determined.
Time frame: 6 weeks
Post operative complications will be assessed through the 6 weeks.
Time frame: 6 weeks
Economic evaluation for inpatient and re-admission will be assessed.
Corewell Health West
Other
Effectiveness of Tranexamic Acid (TXA) in Reducing Blood Loss in Hip Fracture Surgery
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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