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Retroclavicular Versus Costoclavicular Approach for Infraclavicular Brachial Plexus Block

A Randomized Controlled Trial Comparing Retroclavicular and Costoclavicular Approach for Infraclavicular Brachial Plexus Block

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03190551
Enrollment
60
Registered
2017-06-19
Start date
2017-01-31
Completion date
2017-04-30
Last updated
2017-06-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Disorder of Upper Extremity

Keywords

infraclavicular brachial plexus block, retroclavicular approach, costoclavicular approach, upper limb surgery, needle shaft visibility

Brief summary

The primary aim of this study is to compare needle shaft visibility between the retroclavicular approach and costoclavicular approach for infraclavicular brachial plexus block in patients undergoing elective upper limb surgery. Secondary aim is to investigate the differences between the two groups in sensorial block success rate, block performance time, block performance related pain, motor block success rate, surgical success rate, complications, patient satisfaction, use of supplemental local anesthetic, use of analgesic.

Detailed description

Infraclavicular blocks are performed with different approaches. This study evaluated the effectiveness, safety and feasibility of a retroclavicular brachial plexus block as compared with costoclavicular approach for infraclavicular brachial plexus block. 60 patients scheduled for elective upper limb surgery were recruited and randomized into two groups: Retroclavicular approach for infraclavicular block (Group I), costoclavicular approach for infraclavicular block (Group R). Sensory block, adverse effects and complications were evaluated and recorded every 5 minutes until 30 min after local anesthetic injection. Success rate of each nerve sensory block, complications, rate of satisfaction, rate of failure and incidence rate of adverse effects, the needle shaft visibility, procedure time,duration of the block's effect, use of supplemental local anesthetic, use of analgesic are compared with both groups.

Interventions

Retroclavicular approach for ultrasound guided infraclavicular brachial plexus block

costoclavicular approach for ultrasound guided infraclavicular brachial plexus block

Sponsors

Antalya Training and Research Hospital
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Caregiver, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* patients who undergo elective forearm or hand surgery under infraclavicular brachial plexus block * American Society of Anesthesiologists class 1 to 3 * Ability to consent

Exclusion criteria

* History of allergic reaction to local anaesthetics * Peripheral neuropathy * Renal or hepatic insufficiency * Coagulation disorders

Design outcomes

Primary

MeasureTime frameDescription
Needle shaft visibility10 minutes after the needle inserted the skinNeedle visibility reviewed by two anesthesiologists using a 5-point Likert scale

Secondary

MeasureTime frameDescription
supplemental analgesic used90 minutes after block completionThe use of supplementary local anesthetic and the use of intravenous narcotics were recorded.
Technique durationTime required in seconds for the block completion (10 minutes)Number of seconds needed to complete the block, from time of local skin anesthesia until regional block needle removal.
complications such as pneumothorax, hemothorax, intraarterial injection, intravenous injection24 hoursAsked about possible complications
Patient satisfaction using a visual analogue scaleAssessed 24 hours after the blockUsing a visual analog scala, patients will quantify their satisfaction with the retroclavicular and costaclavicular technique .
Success Rate of the sensorial BlockAssessed 30 minutes after block completionSuccess is defined as complete sensory loss in the distribution of the radial, median, ulnar, musculocutaneous, and medial cutaneous nerves of the forearm and hand
Block performance related pain10 minutes after the needle inserted the skinBlock performance related pain was evaluated with a visual analog scala after the removal of the needle.
motor block success rateAssessed 40 minutes after block completionSuccess is defined as complete motor block in the distribution of the radial, median, ulnar, musculocutaneous nerves of the forearm and hand

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026