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 @ 4:02 PM
Ignite Modification Date: 2025-12-24 @ 4:02 PM
NCT ID: NCT01096966
Eligibility Criteria: Inclusion Criteria: 1. Diagnosis of chronic low back pain for more than 3 months 2. If taking non-steroidal anti-inflammatory drugs or non-opioid analgesics, must be on a regular, scheduled dose for at least 4 weeks prior to the first visit and intend to remain on a stable dose of these agents for the study duration 3. Pain intensity score greater than or equal to 5 out of 10 at the first visit 4. Able to apply patches at home 5. Able and willing to complete daily pain intensity ratings using an electronic diary device for the duration of the study 6. Females of childbearing potential must agree to use a medically acceptable method of contraception throughout the study Exclusion Criteria: 1. History of, or ongoing, alcohol or drug abuse 2. Positive drug test for alcohol, illicit drug use or opioids 3. Primary diagnosis of chronic low back pain due to neuropathic pain 4. History of back surgery or plan for back surgery 5. Use of opioids within 2 weeks of the first visit and during the study 6. Previous ineffective use of lidocaine patches 7. Morbid obesity 8. Moderate or severe depression 9. An open skin lesion within the painful area where patches will be applied 10. Patients with active or resolved back pain litigation or receiving disability payments due to chronic low back pain 11. Pregnant or breastfeeding females
Healthy Volunteers: False
Sex: ALL
Minimum Age: 18 Years
Maximum Age: 70 Years
Study: NCT01096966
Study Brief:
Protocol Section: NCT01096966