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Clinical Trials/NCT07151443
NCT07151443
Recruiting
Not Applicable

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

Ankara Etlik City Hospital1 site in 1 country60 target enrollmentStarted: September 15, 2025Last updated:

Overview

Phase
Not Applicable
Status
Recruiting
Sponsor
Ankara Etlik City Hospital
Enrollment
60
Locations
1
Primary Endpoint
Block Performance Time

Overview

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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 80 Years (Adult, Older Adult)
Sex
All
Accepts 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

Outcomes

Primary Outcomes

Block Performance Time

Time Frame: During regional anesthesia

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

Secondary Outcomes

  • Pain Score(Up to 24 hours)
  • Patient Satisfaction(1 day)

Investigators

Sponsor
Ankara Etlik City Hospital
Sponsor Class
Other Gov
Responsible Party
Principal Investigator
Principal Investigator

İbrahim Topcu

Principal Investigator

Ankara Etlik City Hospital

Study Sites (1)

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