Pain Blocking During Drug Administration or Blood Collection With Needles
This study is enrolling participants by invitation only.
Sponsor:
Montana Compton
Information provided by (Responsible Party):
Montana Compton, University of California, Irvine
ClinicalTrials.gov Identifier:
NCT01166906
First received: July 20, 2010
Last updated: January 7, 2013
Last verified: January 2013
| Tracking Information | |||||
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| First Received Date ICMJE | July 20, 2010 | ||||
| Last Updated Date | January 7, 2013 | ||||
| Start Date ICMJE | March 2010 | ||||
| Estimated Primary Completion Date | March 2013 (final data collection date for primary outcome measure) | ||||
| Current Primary Outcome Measures ICMJE |
Pain Blocking During Drug Administration or Blood Collection With Needles [ Time Frame: up to 12 months ] [ Designated as safety issue: No ] Pain Blocking During Drug Administration or Blood Collection With Needles |
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| Original Primary Outcome Measures ICMJE | Not Provided | ||||
| Change History | Complete list of historical versions of study NCT01166906 on ClinicalTrials.gov Archive Site | ||||
| Current Secondary Outcome Measures ICMJE | Not Provided | ||||
| Original Secondary Outcome Measures ICMJE | Not Provided | ||||
| Current Other Outcome Measures ICMJE | Not Provided | ||||
| Original Other Outcome Measures ICMJE | Not Provided | ||||
| Descriptive Information | |||||
| Brief Title ICMJE | Pain Blocking During Drug Administration or Blood Collection With Needles | ||||
| Official Title ICMJE | Pain Blocking During Drug Administration or Blood Collection With Needles | ||||
| Brief Summary | The researcher at UCI Beckman Laser Institute develop pain blocking device to study the level of pain prior to and during drug administration or blood collection by needles. |
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| Detailed Description | The pain blocking device can block the pain before and during injection. This method can be well-controlled and low-cost method to relieve pain without direct solid contact with the skin. The standard pain scale will be collected with this study. |
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| Study Type ICMJE | Observational | ||||
| Study Design ICMJE | Observational Model: Case-Only Time Perspective: Prospective |
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| Target Follow-Up Duration | Not Provided | ||||
| Biospecimen | Not Provided | ||||
| Sampling Method | Non-Probability Sample | ||||
| Study Population | primary care clinic, community sample, |
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| Condition ICMJE | Pain, Intractable | ||||
| Intervention ICMJE | Device: pain blocking
pain blocking |
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| Study Group/Cohort (s) | Not Provided | ||||
| Publications * | Not Provided | ||||
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* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. |
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| Recruitment Information | |||||
| Recruitment Status ICMJE | Enrolling by invitation | ||||
| Estimated Enrollment ICMJE | 100 | ||||
| Estimated Completion Date | March 2013 | ||||
| Estimated Primary Completion Date | March 2013 (final data collection date for primary outcome measure) | ||||
| Eligibility Criteria ICMJE | Inclusion Criteria:
Exclusion Criteria:
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| Gender | Both | ||||
| Ages | 18 Years and older | ||||
| Accepts Healthy Volunteers | Yes | ||||
| Contacts ICMJE | Contact information is only displayed when the study is recruiting subjects | ||||
| Location Countries ICMJE | United States | ||||
| Administrative Information | |||||
| NCT Number ICMJE | NCT01166906 | ||||
| Other Study ID Numbers ICMJE | NIH NIBIB;HS#2009-7245 | ||||
| Has Data Monitoring Committee | No | ||||
| Responsible Party | Montana Compton, University of California, Irvine | ||||
| Study Sponsor ICMJE | Montana Compton | ||||
| Collaborators ICMJE | Not Provided | ||||
| Investigators ICMJE |
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| Information Provided By | University of California, Irvine | ||||
| Verification Date | January 2013 | ||||
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ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP |
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