Injection Site in Ultrasound-Guided Interscalene Block for Shoulder Arthroscopy

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorSultan Abdulhamid Han Training and Research Hospital, Istanbul, Turkey

About this trial

Ultrasound-guided interscalene block is commonly used for postoperative analgesia in patients undergoing shoulder arthroscopy. The location of local anesthetic injection may influence both block efficacy and the incidence of block-related complications. This randomized, double-blind clinical trial compares two different injection sites around the C5-C7 nerve roots using the same local anesthetic dose and volume. The study will assess block success, postoperative analgesia, opioid consumption, diaphragmatic function, and procedure-related complications.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

None

Disqualifiers

None

Trial design

Design model

Parallel

Treatments tested in this trial

  • Ultrasound-Guided Interscalene Block

    Procedure/Surgery

    Ultrasound-guided interscalene brachial plexus block performed before induction of general anesthesia. Participants are assigned to one of two injection sites around the C5-C7 nerve roots according to the randomized study protocol.

Treatment groups

50 Participants
are divided into 2 treatment groups
Group A: Anterior Interscalene BlockExperimental treatment 1 intervention
Group B: Posterior Interscalene BlockExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Postoperative Analgesic Efficacy

Postoperative analgesic efficacy will be assessed using patient-controlled analgesia demand and delivered dose counts and the need for rescue analgesia.

Time frame
12 hours after surgery

Secondary outcomes

1

Time to First Rescue Analgesic

Time from the end of surgery to first rescue analgesic administration.

Time frame
12 hours after surgery
2

Hemidiaphragmatic Paralysis

Presence of ipsilateral hemidiaphragmatic paralysis assessed by ultrasonography.

Time frame
Before block and 2 hours after surgery
3

Block-Related Complications

Incidence of vascular puncture, intraneural injection, Horner syndrome, dyspnea, hoarseness, nausea, vomiting, recurrent laryngeal nerve block, stellate ganglion block, and prolonged motor block.

Time frame
During block placement and within 12 hours after surgery
4

Block Duration

Duration of sensory and motor block recorded during postoperative follow-up.

Time frame
12 hours after surgery

Other outcomes

Sponsors and contacts

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