Efficacy of Variable Volume Truncal Blocks in Upper Limb Orthopedic Surgery
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorGaziosmanpasa Research and Education Hospital
About this trial
aim of this study is to compare the effect of selective truncal blocks, performed at different doses and volumes, on the onset times of motor and sensory blocks required for anesthesia in patients scheduled for hand, wrist, forearm, and elbow surgeries. Completing the operation under regional anesthesia will be considered a successful block.
Eligibility criteria
Qualifiers
ASA 1-2
Body Mass Index (BMI) of 18-35 kg/m²
Age: 18-65 years -Patients undergoing all upper extremity orthopedic surgeries, except shoulder surgeries (distal humerus, elbow, forearm, hand, and wrist), will be included. -
Disqualifiers
Patient refusal
Pregnancy or breastfeeding
Severe pulmonary disease
Contralateral diaphragm paralysis
Trial design
Treatments tested in this trial
- Selective turuncus block with 25 ml bupivacain
- Selective turuncus block with 15 ml bupivacain
Treatment groups
60 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov