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 @ 7:18 PM
Ignite Modification Date:
2025-12-24 @ 7:18 PM
NCT ID:
NCT02496403
Eligibility Criteria:
Inclusion Criteria:
* inducted for buprenorphine/naloxone treatment at the Sacramento CDRP
* diagnosis of opioid dependence
* English speaking
* Willing and able to be randomized to treatment arm
Exclusionary criteria:
* dementia
* mental retardation
* actively psychotic or suicidal
* medically unstable
* using opioids
* pregnant women
* inducted on bup/nx for chronic pain
* inducted on bup/nx for detoxification purposes only
* enrolled in DDIOP, residential treatment or day treatment
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT02496403
Study Brief:
Protocol Section:
NCT02496403