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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01166906
Other study ID # 20097245
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 2010
Est. completion date March 2014

Study information

Verified date October 2022
Source University of California, Irvine
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

There is a gating mechanism in the dorsal horn of the spinal cord that acts to facilitate or inhibit transmission of pain signals to the brain. The gate can be closed by mechanical stimuli such as touch and vibration.


Description:

The researcher develope a device that can use to reduce pain during drug administration or blood collection with needles.


Recruitment information / eligibility

Status Completed
Enrollment 53
Est. completion date March 2014
Est. primary completion date March 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Receiving an injection with a needle - Able to score the pain on a scale of 0-10 using the universal pain assessment tool, preferably 7 years of age or older Exclusion Criteria: - Current pregnancy - Inability to understand and carry out instruction

Study Design


Related Conditions & MeSH terms


Intervention

Device:
pain blocking
pain blocking

Locations

Country Name City State
United States Beckman Laser Institute Medical clinic Irvine California

Sponsors (2)

Lead Sponsor Collaborator
University of California, Irvine Beckman Laser Institute University of California Irvine

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain Blocking During Drug Administration or Blood Collection With Needles Pain Blocking During Drug Administration or Blood Collection With Needles up to 12 months
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