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

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

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07151443
Enrollment
60
Registered
2025-09-03
Start date
2025-09-15
Completion date
2026-06-25
Last updated
2025-12-15

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

Conditions

Forearm Surgery, Hand Surgery, Pain Management, Peripheral Nerve Block, Upper Extremity

Keywords

Infraclavicular Block, Obesity, Upper Extremity, Hand surgery, Forearm surgery

Brief summary

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.

Interventions

PROCEDUREConventional approach to infraclavicular block

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.

PROCEDURERetroclavicular approach to the infraclavicular block

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.

Sponsors

Ankara Etlik City Hospital
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* 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

Exclusion criteria

* Patients who cannot perceive and evaluate pain * Patients who want to have surgery under general anesthesia * Patients in whom regional anesthesia is contraindicated

Design outcomes

Primary

MeasureTime frameDescription
Block Performance TimeDuring regional anesthesiaTotal block performance time (from skin puncture to needle removal) will be recorded

Secondary

MeasureTime frameDescription
Pain ScoreUp to 24 hoursPain 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.
Patient Satisfaction1 dayQuality 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.

Countries

Turkey (Türkiye)

Contacts

Primary ContactIbrahim Topcu, MD
ibrahimtpc78@gmail.com+905437860316
Backup ContactMusa Zengin, Associate Professor
musazengin@gmail.com+905307716235

Outcome results

None listed

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