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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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19 February 2015 |
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Main ID: |
NCT01404468 |
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Date of registration:
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21/07/2011 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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The Phonophoresis of Lidocaine Gel and Its Effect on Sensory Blockage
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Scientific title:
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Effect of Lidocaine Phonophoresis on Sensory Blockade: Pulsed or Continuous Mode of Therapeutic Ultrasound? |
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Date of first enrolment:
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March 2006 |
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Target sample size:
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93 |
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Recruitment status: |
Completed |
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URL:
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http://clinicaltrials.gov/show/NCT01404468 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Basic Science
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Phase:
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Phase 0
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Countries of recruitment
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Iran, Islamic Republic of
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Contacts
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Name:
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samaneh ebrahimi, PhD student |
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Address:
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Telephone:
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Email:
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Affiliation:
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PhD student in shiraz university of medical sciences |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Men and women aged 18 to 25 years
Exclusion Criteria:
- individuals who had a disease that could affect the experiment, such as systemic
disease,impairment of the sensory system(e.g.neuropathy,diabetes),cardiovascular
disorders(e.g. increased blood pressure),pain due to an injury to the upper
extremity,tumours,malignant and precancerous tissue,acute infection and broken skin
in the area; and individuals taking medication to relieve disease symptoms were
excluded
Age minimum:
18 Years
Age maximum:
28 Years
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Impairment, Light Touch Sensation
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Pain
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Intervention(s)
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Device: continuous ultrasound device with lidocaine
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Other: off device
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Device: pulsed ultrasound device with lidocaine
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Primary Outcome(s)
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Two-point discrimination,touch and maximum pain thresholds
[Time Frame: imediately after finishing the application of ultrasound (5 minutes after intervention)]
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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