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Infrared Thermography to Evaluate the Effect of Paravertebral Block

Changes of Skin Temperature for Evaluation of Paravertebral Block: A Prospective Observational Study Using Infrared Thermography

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04078347
Enrollment
61
Registered
2019-09-06
Start date
2019-10-01
Completion date
2020-10-31
Last updated
2021-01-12

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

Conditions

Paravertebral Block

Keywords

Paravertebral block, Infrared thermography

Brief summary

The aim of this prospective observational study was to evaluate the changes of skin temperature after the paravertebral block measured by infrared thermography.

Detailed description

Methods: Patients scheduled for elective surgery with paravertebral block will receive infrared thermography measures 5 min before the block and continous to 20 min after the block. The sensitivity, specificity of infrared thermography as diagnostic methods will be determined by receiver operator characteristic analysis.

Interventions

PROCEDUREParavertebral block at T4 and T5 level

Paravertebral block is performed at T4 and T5 level under realtime ultrasound guidenance with 10ml of 0.5% ropivacaine for each block, respectively.

Sponsors

Huazhong University of Science and Technology
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years

Inclusion criteria

* With informed consent * American Society of Anesthesiologists physical status Ⅰ-Ⅱ * Undergo elective surgery with planned paravertebral block

Exclusion criteria

* Refusal to participate in the study * pre-existing infection at the block site * younger than 18-yr-old * BMI\>35 * significant thoracic kyphoscoliosis * Those who had taken vasodilatory drugs before surgery * history of previous thoracic or breast surgery * Preoperative analgesic medications * Any contraindications to peripheral nerve block such as coagulation abnormalities, allergy to local anaesthetics, peripheral neuropathy.

Design outcomes

Primary

MeasureTime frameDescription
Changes of skin temperatureFrom baseline up to 20 minutes after blockChanges of skin temperature determined by infrared thermography

Secondary

MeasureTime frameDescription
Noinvasive blood pressureFrom baseline up to 20 minutes after blockVital signs
Heart rateFrom baseline up to 20 minutes after blockVital signs
SPO2From baseline up to 20 minutes after blockvital signs
Sensory block levelFrom baseline up to 20 minutes after blockSensory block level determined by pinprick.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 22, 2026