Last updated: November 21, 2024
Sponsor: Istanbul University
Overall Status: Completed
Phase
N/A
Condition
N/ATreatment
Ultrasonographic measurement of diaphragm thickness
Clinical Study ID
NCT06329440
2023/880
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- adult patients who will undergone upper extremity peripheral block
Exclusion
Exclusion Criteria:
coagulation disorders
paediatric patients
Patients who do not accept regional anaesthesia
known local anaesthetic allergy
Patients who are under anticoagulant therapy
Pregnancy
Study Design
Total Participants: 50
Treatment Group(s): 1
Primary Treatment: Ultrasonographic measurement of diaphragm thickness
Phase:
Study Start date:
April 01, 2024
Estimated Completion Date:
November 21, 2024
Connect with a study center
Istanbul University Istanbul Faculty of Medicine
Istanbul,
TurkeySite Not Available
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