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Blood Flow Index as an Indicator of Successful Peripheral Nerve Block

H

Huazhong University of Science and Technology

Status

Completed

Conditions

Laser

Study type

Observational

Funder types

Other

Identifiers

NCT03169517
TJMZK20170325

Details and patient eligibility

About

Laser speckle contrast imaging (LSCI) allows real-time, non-invasive, quantitative measurements of regional blood flow. The aim of this prospective observational study was to evaluate the blood flow changes by LSCI after peripheral nerve block and determine whether this novel optical technique can be used as a reliable indicator of successful blocks.

Full description

Methods: One hundred adult patients scheduled for elective upper or lower limb surgery with peripheral nerve block will receive LSCI measurements and pinprick sensory tests before the block and at 5-min intervals till 30 min after the block. The sensitivity, specificity of LSCI as a diagnostic method will be determined by receiver operator characteristic analysis.

Clinical Implications: LSCI with quantitative data could be used as an indicator of successful blocks.

Enrollment

110 patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • informed consent
  • American Society of Anesthesiologists physical statusⅠ-Ⅱ
  • Undergo elective upper or lower limb surgery with peripheral nerve block

Exclusion criteria

  • refusal to participate in the study
  • peripheral vascular disease
  • digit injury or deficiency
  • colored or infected fingernails/toenails
  • BMI>35
  • those who had taken vasodilatory drugs before surgery
  • preoperative analgesic medications
  • Any contraindications to peripheral nerve block such as coagulation abnormalities, allergy to local anaesthetics, peripheral neuropathy.

Trial design

110 participants in 1 patient group

Peripheral nerve block group
Description:
patients scheduled for elective upper or lower limb surgery with peripheral nerve block will receive LSCI measurements and pinprick sensory tests at 5 min before the block and at 5-min intervals till 30 min after the block.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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