Pain Blocking During Drug Administration or Blood Collection With Needles
NCT ID: NCT01166906
Last Updated: 2022-11-01
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
53 participants
OBSERVATIONAL
2010-03-31
2014-03-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Impact of Vibrating Device Distraction on Mechanical Pain Thresholds Induced by Needle Sham
NCT06271642
Technical Efficacy of a Direction Specific Radiofrequency Device in the Performance of Lumbar Medial Branch Neurotomies
NCT02120625
Brain Network Stimulation for Chronic Low Back Pain.
NCT06902233
Back Pain Response to Different Acupuncture Methods
NCT01598974
Dry Needling at the Thoracolumbar Junction on Measures of Sympathetic Outflow and Flexibility
NCT03630172
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_ONLY
PROSPECTIVE
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
pain blocking
pain blocking
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* 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
* Inability to understand and carry out instruction
18 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Beckman Laser Institute University of California Irvine
OTHER
University of California, Irvine
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Beckman Laser Institute and Medical Center
Wangcun Jia, PhD., Research Scientist
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Wangcun Jia, PhD
Role: PRINCIPAL_INVESTIGATOR
Beckman Laser Institute University of California Irvine
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Beckman Laser Institute Medical clinic
Irvine, California, United States
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
20097245
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.