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Clinical Trials/NCT07326436
NCT07326436CompletedNot Applicable

Comparison of Sympathetic Block Duration and Rebound Sympathetic Activity Rate in Infraclavicular and Supraclavicular Brachial Plexus Blocks Using Perfusion Index and Skin Temperature

Bozyaka Training and Research Hospital1 site in 1 country200 target enrollmentStarted: March 1, 2023Last updated:
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
200
Locations
1
Primary Endpoint
Difference in duration of sympathetic blockade after different US-guided brachial plexus blocks

Study Overview

Brief Summary

This prospective comparative study will evaluate the sympathetic effects of ultrasound-guided infraclavicular versus supraclavicular brachial plexus blocks in adults undergoing upper-extremity surgery. Sympathetic tone will be monitored noninvasively with simultaneous bilateral measurements of perfusion index (pulse-oximetry-derived) and skin temperature obtained at baseline and at predefined post-block intervals until return to baseline. The primary outcome is the duration of sympathetic block. Secondary outcomes are between-approach differences in the time course of perfusion index and skin temperature, and the incidence and magnitude of rebound sympathetic activity.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
Double (Investigator, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • 18 to 65 year old
  • Patients scheduled for upper extremity surgery
  • Fully oriented and able to cooperate
  • Patients who signed the informed consent form and gave consent to participate in the study

Exclusion Criteria

  • ASA III-IV-V
  • Non-cooperation
  • Disease that interferes with sensory block assessment
  • Known allergy to the medicines to be used
  • Pregnant patients
  • Coagulopathy or thrombocytopenia
  • Patients with anatomical abnormalities or active infection at the points of application

Arms & Interventions

Supraclavicular brachial plexus block

Active Comparator

Intervention: Supraclavicular brachial plexus block (Procedure)

Infraclavicular brachial plexus block

Active Comparator

Intervention: Infraclavicular brachial plexus block (Procedure)

Outcomes

Primary Outcomes

Difference in duration of sympathetic blockade after different US-guided brachial plexus blocks

Time Frame: Twenty-four hours after nerve blockage

Secondary Outcomes

  • Change in perfusion index between infraclavicular and supraclavicular approaches(Twenty-four hours after nerve blockage)

Investigators

Sponsor
Bozyaka Training and Research Hospital
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Pelin Doğan Uzun

Doctor of medicine

Bozyaka Training and Research Hospital

Study Sites (1)

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