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Not yet recruiting NCT07369843

LASER Effects Blood Flow

No phase Interventional Pain Management

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: physical therapy (low power LASER).
Who it may be relevant to
Registry conditions: Pain Management. Basic parameters: 20 years — 45 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Effects of Low Power LASER on the Heart Rate Variability of Human Subjects

Overview

This study investigate the potential impact of low power laser (LPL), an non-invasive physical therapy, on the cardiovascular system by focusing on its effect on heart rate and autonomic tone. Study will recruit healthy volunteers and non-invasively monitor their electrocardiogram and digital pulse in response to LPL. In addition, the potential involvement of autonomic tone will be clarify by topically applying gel (2% lidocaine gel)

Detailed description

This study investigate the potential impact of low power laser (LPL), an non-invasive physical therapy, on the cardiovascular system by focusing on its effect on heart rate and autonomic tone.

Study will recruit healthy volunteers (age 20-60; having no diabetes, hypertension, or other medical problem) and non-invasively monitor their electrocardiogram and digital pulse in response to LPL (with an intensity for relieving pain).

In addition, the potential involvement of autonomic tone will be clarify by topically applying gel (2% lidocaine gel) at the site 2 cm distal to the applying site.

Interventions

  • Other physical therapy (low power LASER)
    Low power laser with an intensity for pain relieving will be applied to volunteers

Primary outcome measures

  • heart rate [Time frame: Continuous heart rate (HR) recording will start when it is stable after a brief resting (10 min); maintained during stimulation (30 min), and lasted for a period until the HR recovers.]

Eligibility criteria

Inclusion criteria

  • age from 20-45

Exclusion criteria

  • no medical history of diabetes, hypertension, or other medical problem

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Basic science

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07369843 · LASERBF1 · Saint Paul's Hospital

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗