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OpenTrials
Completed

NCT Number: NCT01166906

Pain Blocking During Drug Administration or Blood Collection With Needles

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Beckman Laser Institute Medical clinic

Irvine, California, 92612, United States

About this study

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

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

pain blocking

Device

pain blocking

Primary outcomes

  1. 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

Sponsors and collaborators

Lead sponsor

University of California, Irvine

Other

Collaborators

  • Beckman Laser Institute University of California Irvine

Registry information

Important dates

Study start
2010
Primary completion
2014
Study completion
2014
First posted
Jul 21, 2010
Registry last updated
Nov 1, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.