Eligibility Module

Eligibility Module

The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.

Eligibility Module path is as follows:

Study -> Protocol Section -> Eligibility Module

Eligibility Module


Ignite Creation Date: 2025-12-24 @ 7:17 PM
Ignite Modification Date: 2025-12-24 @ 7:17 PM
NCT ID: NCT00978003
Eligibility Criteria: * INCLUSION CRITERIA: 1. Healthy male and female volunteers between the ages of 18 and 55. \<TAB\> EXCLUSION CRITERIA: 1. Any relevant medical problems (connective tissue problems, active arthritis, etc.) 2. Any clinical signs of a knee impairment in the joint being studied, including abnormal range of motion, muscle weakness, malaligment, and ligament damage. 3. Any serious injury to the joint being studied, previous surgery on the joint being studied or extreme pain at the joint being studied. 4. Allergy/hypersensitivity to lidocaine. 5. Liver disease. 6. Open angle glaucoma. 7. Cardiac arrhythmias, congenital heart disease. 8. G6PD. 9. Any female who is pregnant. A volunteer will be excluded if they have a contraindication to MR imaging. Examples include: 1. Metal within their body, which might be expected to concentrate radiofrequency fields or cause tissue damage from twisting in a magnetic field (e.g., aneurysm clip, implanted neural stimulator, implanted cardiac pacemaker or autodefibrillator, cochlear implant, ccular foreign body (e.g. metal shavings, insulin pump). 2. A condition, which would preclude them from participating in an MR imaging study (e.g., paralyzed hemidiaphragm, morbid obesity, severe claustrophobia). 3. A condition that presents an unnecessary risk to them or their unborn child (e.g., pregnancy, previous surgery of uncertain type, symptoms of pheochromocytoma or insulinoma).
Healthy Volunteers: False
Sex: ALL
Minimum Age: 18 Years
Maximum Age: 55 Years
Study: NCT00978003
Study Brief:
Protocol Section: NCT00978003