Comparison of Conventional and Retroclavicular Approaches for Ultrasound-guided Infraclavicular Brachial Plexus Block

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-80
SponsorAnkara Etlik City Hospital

About this trial

Forearm and hand surgeries are among the most frequently performed surgical interventions both in trauma patients and electively.In these procedures, alternative anesthesia methods such as general anesthesia, regional intravenous anesthesia, regional peripheral nerve blocks and local anesthesia are available.

Peripheral nerve blockade can be used for anesthesia and analgesia.This method allows patients to undergo surgery without general anesthesia and increases patient satisfaction by providing effective analgesia in the postoperative period.

The aim of this study was to compare the conventional and retroclavicular approaches to infraclavicular block in patients undergoing forearm and hand surgery.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients 18-80 years of age

Those with ASA score II-III

Those with a body mass index (BMI) >30

Patients who are suitable for forearm and hand surgery under regional anesthesia in the operating room

Disqualifiers

Patients who cannot perceive and evaluate pain

Patients who want to have surgery under general anesthesia

Patients in whom regional anesthesia is contraindicated

Trial design

Design model

Parallel

Treatments tested in this trial

  • Conventional approach to infraclavicular block

    Procedure/Surgery

    Conventional approach to infraclavicular block will be performed on the patients using 20 ml of 0.5% bupivacaine 5ml of %2 lidocaine under ultrasound guidance.

  • Retroclavicular approach to the infraclavicular block

    Procedure/Surgery

    Retroclavicular approach to the infraclavicular block will be performed on the patients using 20 ml of 0.5% bupivacaine 5ml of %2 lidocaine under ultrasound guidance.

Treatment groups

60 Participants
are divided into 2 treatment groups
Group A: Conventional approach to infraclavicular blockActive comparator 1 intervention
Group B: Retroclavicular approach to the infraclavicular blockActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Block Performance Time

Total block performance time (from skin puncture to needle removal) will be recorded

Time frame
During regional anesthesia

Secondary outcomes

1

Pain Score

Pain will be assessed using a visual analog scale from 0 mm (no pain) to 100 mm (worst pain) at rest and when coughing. Pain assessment will be made at 0, 1, 6, 12, 18, and 24 hours after surgery.

Time frame
Up to 24 hours
2

Patient Satisfaction

Quality of recovery-15 (QoR-15) score was used as the satisfaction score. The patient-reported Turkish QoR-15 score includes 15 questions that evaluate the patient's postoperative recovery. The QoR-15 score is grouped under two groups, A and B. A high QoR-15 score, a score between 0 (poor) and 10 (excellent) for each item, and a total score of 150 indicate better quality of recovery.

Time frame
1 day

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.