- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01166906
Pain Blocking During Drug Administration or Blood Collection With Needles
October 28, 2022 updated by: Beckman Laser Institute and Medical Center, University of California, Irvine
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.
Study Overview
Detailed Description
The researcher develope a device that can use to reduce pain during drug administration or blood collection with needles.
Study Type
Observational
Enrollment (Actual)
53
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
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California
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Irvine, California, United States, 92612
- Beckman Laser Institute Medical Clinic
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-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
primary care clinic, community sample,
Description
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 Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Case-Only
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Pain Blocking During Drug Administration or Blood Collection With Needles
Time Frame: up to 12 months
|
Pain Blocking During Drug Administration or Blood Collection With Needles
|
up to 12 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Wangcun Jia, PhD, Beckman Laser Institute University of California Irvine
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
March 1, 2010
Primary Completion (Actual)
March 1, 2014
Study Completion (Actual)
March 1, 2014
Study Registration Dates
First Submitted
July 20, 2010
First Submitted That Met QC Criteria
July 20, 2010
First Posted (Estimate)
July 21, 2010
Study Record Updates
Last Update Posted (Actual)
November 1, 2022
Last Update Submitted That Met QC Criteria
October 28, 2022
Last Verified
October 1, 2022
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 20097245
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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