NCT07151443 Comparison of Conventional and Retroclavicular Approaches for Ultrasound-guided Infraclavicular Brachial Plexus Block
| NCT ID | NCT07151443 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Ankara Etlik City Hospital |
| Condition | Peripheral Nerve Block |
| Study Type | INTERVENTIONAL |
| Enrollment | 60 participants |
| Start Date | 2025-09-15 |
| Primary Completion | 2026-06-05 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 60 participants in total. It began in 2025-09-15 with a primary completion date of 2026-06-05.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
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.
Eligibility Criteria
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
Contact & Investigator
Frequently Asked Questions
Who can join the NCT07151443 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, up to 80 Years, studying Peripheral Nerve Block. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07151443 currently recruiting?
Yes, NCT07151443 is actively recruiting participants. Contact the research team at ibrahimtpc78@gmail.com for enrollment information.
Where is the NCT07151443 trial being conducted?
This trial is being conducted at Yenimahalle, Turkey (Türkiye).
Who is sponsoring the NCT07151443 clinical trial?
NCT07151443 is sponsored by Ankara Etlik City Hospital. The trial plans to enroll 60 participants.