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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06165757
Other study ID # Noise and pain sensitivit
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 10, 2023
Est. completion date January 20, 2024

Study information

Verified date October 2023
Source The Second Affiliated Hospital of Chongqing Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Study the effects of 60dB and 80dB white noise, 50-70dB and 70-90dB non harmonic tones on the basic pain threshold of subjects, including the threshold and tolerance of electrical stimulation pain,the threshold and tolerance of cold pain stimulation, and the threshold and tolerance of tenderness stimulation.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date January 20, 2024
Est. primary completion date January 20, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 35 Years
Eligibility Inclusion Criteria: - Between the ages of 18 and 35, regardless of gender - No serious chronic diseases - There is no self-reported history of chronic opioid drug use or neuropathy Exclusion Criteria: - A history of alcohol or drug abuse - Pregnant or lactating - Severe cardiovascular, kidney, or liver diseases

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
noise stimulation
Apply non harmonic and white noise sound stimuli to the subjects, and then measure the threshold and tolerance values of pressure pain, cold pain, and electrical pain.

Locations

Country Name City State
China Department of Anesthesiology, The Second Affiliated Hospital, Chongqing Medical University Chongqing Chongqing

Sponsors (1)

Lead Sponsor Collaborator
The Second Affiliated Hospital of Chongqing Medical University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary mechanical pain sensitivity Each participant was measured using the pressure pain threshold and tolerance (tested by a pressure meter), which lower value present higher pain sensitivity from the study beginning to 30 min after the procedure
Primary cold pain sensitivity Each participant was measured using the cold pain threshold and tolerance (tested by immersion the hand in 4? water), which lower value present higher pain sensitivity from the study beginning to 30 min after the procedure
Primary electrical pain sensitivity Each participant was measured using the cold pain threshold and tolerance (tested by a electrical stimulator), which lower value present higher pain sensitivity from the study beginning to 30 min after the procedure
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