Status:
COMPLETED
The Effectiveness of Ankaferd Blood Stopper in the Management of Traumatic Bleeding
Lead Sponsor:
Haydarpasa Numune Training and Research Hospital
Conditions:
Bleeding Disorder
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
The objective of this study was to prospectively compare effectiveness of Ankaferd Blood Stopper (ABS) with dry sponges in cessation of bleeding in adult trauma cases with external bleeding due to ext...
Detailed Description
This study was planned as a prospective randomized study. After local ethics committee approval, all consecutive patients admitted to the Emergency Department of the Haydarpasa Numune Training \& Rese...
Eligibility Criteria
Inclusion
- Adult patients (18 years-old and above)
- presented with isolated cuts on the extremities
- cuts sized between 1 and 5 centimeters .
Exclusion
- Patients under 18 years of age
- with only superficial abrasions
- with lacerations smaller than 1 cm and larger than 5 cm
- irregular laceration borders or star-like lacerations
- deep lacerations requiring subcutaneous suturing
- lacerations requiring additional interventions such as tendon repair controlled bleeding
- grade III and IV systemic diseases (advanced heart failure, uncontrolled hypertension, etc.) according to American Society of Anesthesiologists (ASA) classification,
- who received radiotherapy or chemotherapy for malignancies within the last three months
- with the history of hematologic diseases such as leukemia
- using medications leading to hemorrhage risk (oral anticoagulants, aspirin, etc.)
- congenital coagulation factor deficiency such as hemophilia
- multiple trauma and abnormal vital signs
Key Trial Info
Start Date :
October 1 2018
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
October 23 2018
Estimated Enrollment :
80 Patients enrolled
Trial Details
Trial ID
NCT03871452
Start Date
October 1 2018
End Date
October 23 2018
Last Update
March 12 2019
Active Locations (1)
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1
Nazmiye Koyuncu
Istanbul, Turkey (Türkiye), 0620