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SPARK Study - Sympathetic Periarterial Radial Block in Healthy Volunteers

SPARK Study - Sympathetic PeriArterial Radial blocK Study

Status
Not yet recruiting
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07429292
Acronym
SPARK
Enrollment
20
Registered
2026-02-24
Start date
2026-05-01
Completion date
2027-04-01
Last updated
2026-04-01

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

Conditions

Healthy Volunteers, Sympathetic Activity

Keywords

Sympathetic Block, Radial Artery, Cold Pressor Test, Periarterial block

Brief summary

The SPARK Study evaluates changes in peripheral sympathetic vasomotor activity following a targeted, ultrasound-guided periarterial sympathetic block of the distal radial artery in healthy volunteers. Autonomic reactivity will be assessed before and after the block using digit-specific pulse-amplitude index and infrared thermography during standardized cold pressor testing.

Interventions

Small-volume injection (5 mL) of 2% lidocaine around radial artery under ultrasound guidance.

Sponsors

Duke University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* Age 18-50 years * ASA physical status I-II * Able to understand and provide informed consent * Able to comply with study procedures and follow-up * Two hands with 5 intact digits and no significant upper extremity injury

Exclusion criteria

* Allergy to lidocaine or similar anesthetics * Allergy to adhesives or ultrasound gel * Neuromuscular, autonomic, or major vascular disorders affecting upper extremities * Peripheral neuropathy * Raynaud's phenomenon or digital ischemia * Coagulopathy or anticoagulation * Active skin infection near block site * Pregnancy * BMI \> 35 kg/m² * Inability to tolerate cold exposure * Any condition interfering with study conduct

Design outcomes

Primary

MeasureTime frameDescription
Pulse amplitude index (PAI)PAI will be measured at: 1) Baseline; 2) after the first cold pressor test at 0, 5, 10, and 15 minutes; 3) after the sympathetic block at 5 and 10 minutes; 4) after the second cold pressor test at 0, 5, 10, and 15 minutes.Pulse Amplitude Index (PAI) is a noninvasive measure of digital perfusion derived from photoplethysmography (PPG) signals recorded from the fingers. PAI reflects changes in pulse waveform amplitude and serves as an indirect marker of peripheral blood flow and sympathetic vasomotor tone. In this study, PAI will be continuously recorded using digital sensors placed on the index and fifth fingers of the hand undergoing periarterial radial block, as well as the contralateral index finger. Measurements will be obtained at baseline, following cold pressor testing, after the periarterial radial block, and following repeat cold pressor testing. Changes in PAI across time points will be used to assess alterations in peripheral perfusion associated with sympathetic modulation.
Hand temperatureThermal images will be obtained at: 1) Baseline; 2) after the first cold pressor test at 0, 5, 10, and 15 minutes; 3) after the sympathetic block at 5 and 10 minutes; 4) after the second cold pressor test at 0, 5, 10, and 15 minutes.Hand temperature is a noninvasive measure of peripheral skin temperature used as an indicator of changes in local blood flow and sympathetic vasomotor activity. In this study, hand temperature will be assessed using infrared thermographic imaging of both hands. Thermal images will be acquired under standardized environmental conditions at baseline, following cold pressor testing, after the periarterial radial block, and following repeat cold pressor testing. Temperature values will be derived from predefined regions of interest on the hands based on arterial territories, and compared across time points to evaluate changes in peripheral perfusion associated with sympathetic modulation.

Secondary

MeasureTime frameDescription
Temporal Changes in Cold Pressor Test-Induced Vasomotor Responses Pre- and Post-BlockData will be obtained at: 1) Baseline; 2) after the first cold pressor test at 0, 5, 10, and 15 minutes; 3) after the sympathetic block at 5 and 10 minutes; 4) after the second cold pressor test at 0, 5, 10, and 15 minutes.Temporal changes in cold pressor test (CPT)-induced vasomotor responses pre- and post-block refer to time-dependent alterations in peripheral vascular tone before and after periarterial radial block-induced sympathetic modulation. In this study, CPT-induced vasomotor responses will be assessed by evaluating changes in pulse amplitude index (PAI) and hand skin temperature across predefined time points. Measurements will be obtained immediately following CPT, and at serial intervals. CPT will be performed before and after the periarterial radial block. Comparisons of these temporal response patterns before and after the block will be used to characterize the effects of sympathetic modulation on peripheral vasoconstriction and vasodilation.
Change in Vasomotor Measures in the Fifth FingerPAI and thermal images will be measured at: 1) Baseline; 2) after the first cold pressor test at 0, 5, 10, and 15 minutes; 3) after the sympathetic block at 5 and 10 minutes; 4) after the second cold pressor test at 0, 5, 10, and 15 minutes.Change in vasomotor measures in the fifth finger refers to alterations in peripheral perfusion and skin temperature measured in the fifth digit ipsilateral to the periarterial radial block, an area predominantly innervated by the ulnar nerve. In this study, the fifth finger will serve as an internal control for comparison with the radial-innervated index finger. Changes will be assessed using pulse amplitude index (PAI) and infrared thermographic imaging. Measurements will be obtained at baseline, following cold pressor testing, after periarterial radial block, and following repeat cold pressor testing. Responses in the ulnar-innervated fifth finger will be used to evaluate regional vasomotor changes and to track potential extension of radial sympathetic modulation to adjacent, non-radial territories.
Change in Vasomotor Measures in the Contralateral Index FingerPAI and thermal images will be measured at: 1) Baseline; 2) after the first cold pressor test at 0, 5, 10, and 15 minutes; 3) after the sympathetic block at 5 and 10 minutes; 4) after the second cold pressor test at 0, 5, 10, and 15 minutes.Change in vasomotor measures in the contralateral index finger refers to alterations in peripheral perfusion and skin temperature measured in the index finger of the hand opposite to the periarterial radial block. This contralateral finger serves as an internal control to account for systemic sympathetic responses to cold pressor testing that are independent of the local effects of the block and to compare sympathetic reactivity between hands. Vasomotor measures will be assessed using pulse amplitude index (PAI) derived from photoplethysmography and infrared thermographic imaging. Measurements will be obtained at baseline, following cold pressor testing, after periarterial radial block, and following repeat cold pressor testing. Changes across time points will be used to distinguish local from systemic vasomotor effects.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORDavid MacLeod

Duke University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 2, 2026