Effect of Remote Local Peripheral Nerve Cooling on Pain of Arterial Puncture

ConditionAcute Pain
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
AgeNot listed
SponsorThe Second Affiliated Hospital of Chongqing Medical University

About this trial

In this project, volunteers will be recruited to cool the superficial skin of the axillary brachial plexus away from the puncture point, resulting in local peripheral nerve cooling, and observe its impact on the pain of arterial puncture.To explore the local peripheral nerve cooling treatment can produce controllable and reversible analgesic effect even if away from the wound, and provide a new nonpharmaceutical analgesic mode for clinical.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

18 ~ 65 years old;

ASA I-II level;

Patients with perioperative invasive arterial blood pressure monitoring;

Right-handed;

Disqualifiers

Patients with a history of musculoskeletal, vascular, neurological or psychiatric disorders;

Patients with a history of diabetes or other systemic diseases

Patients who used any analgesic medication within the month before and during the study;

Patients with a history of smoking, alcohol or drug addiction;

Trial design

Design model

Parallel

Treatments tested in this trial

  • Skin cooling to 20°C

    Procedure/Surgery

    According to the group, copper parts at a constant temperature of 20°C were placed on the superficial skin of the brachial plexus for 15 minutes.

  • Skin cooling to 15°C

    Procedure/Surgery

    According to the group, copper parts at a constant temperature of 15°C were placed on the superficial skin of the brachial plexus for 15 minutes.

  • Skin cooling to 8°C

    Procedure/Surgery

    According to the group, copper parts at a constant temperature of 8°C were placed on the superficial skin of the brachial plexus for 15 minutes.

  • No skin cooling

    Procedure/Surgery

    According to the group, copper parts at room temperature (23°C) were placed on the superficial skin of the brachial plexus for 15 minutes.

Treatment groups

100 Participants
are divided into 4 treatment groups
Group A: Skin cooling to 20°CExperimental treatment 1 intervention
Group B: Skin cooling to 15°CExperimental treatment 1 intervention
Group C: Skin cooling to 8°CExperimental treatment 1 intervention
Group D: No skin coolingPlacebo comparator 1 intervention

Trial outcomes

Primary outcomes

1

Visual Analogue Pain Scale (VAS) score of arterial puncture procedure

The larger values of the Visual Analogue Pain Scale (VAS) score of local anesthetic injection and the Visual Analogue Pain Scale (VAS) score of arterial puncture catheterization were taken as the Visual Analogue Pain Scale (VAS) score of the process of arterial puncture catheterization.(VAS ranging from 0 to 10, where 0 indicates no pain and 10 indicates the worst pain imaginable)

Time frame
From 0 to 3 hours after the volunteers enter the pre-anesthesia holding area.

Secondary outcomes

1

Pressure pain threshold

Before the start of cooling therapy, 5 minutes into cooling therapy, 15 minutes after the start of cooling therapy, and 10 minutes after rewarming, the handheld algometer is used to measure the Pressure Pain Threshold (PPT) at the following locations: The midpoint of the ulna and radius at the wrist joint of both forearms (as bony pressure pain points) The brachioradialis muscle on the lateral side of the forearm (as muscular pressure pain points) Unit: Kilograms-force per square centimeter (kg/cm²)

Time frame
From 0 to 3 hours after the volunteers enter the pre-anesthesia holding area.
2

Pressure pain tolerance

Before the start of cooling therapy, 5 minutes into cooling therapy, 15 minutes after the start of cooling therapy, and 10 minutes after rewarming, the handheld algometer is used to measure the Pressure Pain Tolerance (PTO) at the aforementioned locations. Unit: Kilograms-force per square centimeter (kg/cm²)

Time frame
From 0 to 3 hours after the volunteers enter the pre-anesthesia holding area.
3

The average perfusion

Before the administration of local anesthesia, during the process of local anesthesia, after the completion of local anesthesia, before arterial puncture, during the arterial puncture procedure, and after the completion of arterial puncture, the patient is instructed to maintain a calm state and lie in a supine position with the left arm abducted. Under these conditions, the Region of Interest (ROI) is outlined using laser speckle technology, and the average perfusion of this area is measured.

Time frame
From 0 to 3 hours after the volunteers enter the pre-anesthesia holding area.
4

The median perfusion

Before the administration of local anesthesia, during the process of local anesthesia, after the completion of local anesthesia, before arterial puncture, during the arterial puncture procedure, and after the completion of arterial puncture, the patient is required to remain calm and in a supine position with the left arm abducted. Under these conditions, the Region of Interest (ROI) is outlined using laser speckle technology, and the median perfusion of this area is measured.

Time frame
From 0 to 3 hours after the volunteers enter the pre-anesthesia holding area.

Other outcomes

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