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An Observational Study of Environmental and SocioEconomic Factors in Opioid Recovery
NCT03604861 · View on ClinicalTrials.gov ↗
Study Summary
The RECOVER Study will examine clinical, environmental and socioeconomic factors in recovery from opioid use disorder (OUD) over a 24-month period following exit from a Phase III clinical program for a buprenorphine extended-release injection (RBP-6000). The study population will consist of participants from studies NCT02357901 (RB-US-13-0001) and NCT02510014 (RB-US-13-0003). The RECOVER study will characterize OUD subjects' recovery process as they transition from the controlled clinical trial environment to the real world setting.
Conditions Studied
Interventions
- OTHER Not applicable - no defined intervention
Study Locations (20)
Florida
- Amit Vijapura — Jacksonville
- Meridien Research — Lakeland
- Try Research — Maitland
- Innovative Clinical Research — Miami
- Scientific Clinical Research — Miami
- Research Centers of America — Oakland Park
California
- Behavioral Research Specialists — Glendale
- Collaborative Neuroscience Networks, Inc. — Long Beach
- Synergy Research Center — National City
- North County Clinical Research — Oceanside
- Artemis Institute for Clinical Research — San Diego
Alabama
- Winston Technology Research LLC — Haleyville
- Boyett Health Services — Hamilton
Louisiana
- Louisiana Research Associates — New Orleans
- Louisiana Clinical Research — Shreveport
Massachusetts
- Stanley Street Treatment and Resources — Fall River
- Adams Clinical Trials — Watertown
Arkansas
- Woodland International Research Group — Little Rock
Mississippi
- Precise Research Centers, Inc. — Flowood
Missouri
- St. Louis Clinical Trials — St Louis
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 534 participants |
| Start Date | 2015-08 |
| Est. Completion | 2019-03 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03604861
The ClinicalTrials.gov registry entry for NCT03604861 describes a study currently listed as completed. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 534 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Indivior, which has 9 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 2 conditions, with Opioid-use Disorder appearing as the primary indexed condition, and to 1 intervention — of which Not applicable - no defined intervention is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT03604861 reports 20 study locations spanning 8 distinct geographic areas — top geographies include Florida, California, Alabama. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT03604861 about?
NCT03604861 is a clinical study titled "An Observational Study of Environmental and SocioEconomic Factors in Opioid Recovery". The RECOVER Study will examine clinical, environmental and socioeconomic factors in recovery from opioid use disorder (OUD) over a 24-month period following exit from a Phase III clinical program for a buprenorphine extended-release injection (RBP-6000). The study population will consist of particip...
What is the current status of trial NCT03604861?
This trial is currently completed. The enrollment target is 534 participants. The study started on 2015-08. Estimated completion is 2019-03.
What conditions does trial NCT03604861 study?
This clinical trial studies the following conditions: Opioid-use Disorder, Opioid-related Disorders. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT03604861?
The interventions under investigation include: Not applicable - no defined intervention (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT03604861?
This trial is sponsored by Indivior, which has 9 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT03604861 being conducted?
This trial has 20 study locations across Alabama, Arkansas, California, Florida, Louisiana. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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