Remote Methadone Ingestion Surveillance Trial (RMIST)
NCT05259501 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 15
Last updated 2025-12-23
Summary
The Remote Methadone Ingestion Surveillance Trial (RMIST) will explore a potential method of methadone ingestion surveillance that may mitigate patient safety risks of take-home methadone treatment regimens while minimizing the risk of diversion and evaluating the acceptability and feasibility of these monitoring methods. The method utilizes an innovative existing technology.
Conditions
Interventions
- OTHER
-
RMIST
RMIST will involve: 1. A study automated visual recognition web-based platform accessible on the participant's smartphone web browser. 2. A supply of methadone in single use bottles and previously described packaging to be kept securely at the methadone clinic/lab setting.
Sponsors & Collaborators
-
National Institute on Drug Abuse (NIDA)
collaborator NIH -
University of Texas Southwestern Medical Center
lead OTHER
Principal Investigators
-
Madhukar H Trivedi, MD · University of Texas Southwestern Medical Center
Study Design
- Allocation
- NA
- Purpose
- HEALTH_SERVICES_RESEARCH
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Max Age
- 65 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2025-01-15
- Primary Completion
- 2025-03-13
- Completion
- 2025-03-13
Countries
- United States
Study Locations
More Related Trials
-
Individual Patient Esmethadone (REL-1017) Expanded Access Program
NCT06009003 ·Status: TEMPORARILY_NOT_AVAILABLE
-
Effects of Switching From Racemic Methadone to R-methadone on QTc Intervals
NCT04254731 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE4
-
Phase 1 Study to Evaluate RDC-0313 Coadministered With Buprenorphine to Opioid-Experienced Healthy Adults
NCT01046539 ·Status: COMPLETED ·Phase: PHASE1
-
Dose Ranging Study in Healthy Methadone Maintenance Subjects
NCT00387491 ·Status: COMPLETED ·Phase: PHASE1
-
A Study to Evaluate Withdrawal Effects Following Dosing of Oxycodone/Naltrexone in Methadone-Maintained Subjects
NCT02391571 ·Status: COMPLETED ·Phase: PHASE3
-
Efficacy of Extended Release Tramadol for Treating Prescription Opioid Withdrawal
NCT00980044 ·Status: COMPLETED ·Phase: PHASE2/PHASE3
-
Clinical Outcomes Following Transcutaneous Auricular Neurostimulation to Improve Relapse Prevention: A Long-term Follow-up Study
NCT05591703 ·Status: COMPLETED
-
Stimulant Overdose in the Medicaid Population: Who is at Risk, and When Are They at Risk
NCT05976984 ·Status: COMPLETED
-
Impact of Bridge™ Device to Treat Opioid Withdrawal Symptoms
NCT05924945 ·Status: TERMINATED ·Phase: NA
-
Delivering Transcutaneous Auricular Neurostimulation to Improve Relapse Prevention in Opioid Use Disorder
NCT05053503 ·Status: COMPLETED ·Phase: NA
-
Study of D-Methadone in Patients With Chronic Pain
NCT00588640 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Evaluation of the Efficacy and Safety of Two Methadone Titration Methods for the Treatment of Cancer-related Pain With Inadequate Pain Relief or Intolerable Side Effects When Treated With Level 3 Opioids.
NCT01793480 ·Status: COMPLETED ·Phase: PHASE3
-
Surveillance Monitoring of Opioid Abuse in Poison and Drug Treatment Centers
NCT02871232 ·Status: UNKNOWN
-
Accuracy of Point of Care (POC) or In-office Urine Drug Testing (Immunoassay) in Chronic Pain Patients
NCT01052155 ·Status: COMPLETED
-
Morphine Slow-release Capsules in Substitution Therapy
NCT01079117 ·Status: COMPLETED ·Phase: PHASE3
-
Determining the Feasibility of Outpatient Parenteral Antibiotic Therapy for Persons Who Inject Opioids
NCT05300581 ·Status: COMPLETED ·Phase: NA
-
Safety, Tolerability and Pharmacokinetics of Single Ascending Doses of REL-1017 (d-Methadone)
NCT03637361 ·Status: COMPLETED ·Phase: PHASE1
-
Optimizing Retention, Duration and Discontinuation Strategies for Opioid Use Disorder Pharmacotherapy (RDD)
NCT04464980 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE2
-
Slow-Release Oral Morphine for the Treatment of Opioid Use Disorder
NCT03948464 ·Status: TERMINATED ·Phase: PHASE3
-
Examine Plasma Concentrations of Buprenorphine Following Reapplication of Buprenorphine Transdermal System (BTDS) After Variable Application Site Rest Periods
NCT01259102 ·Status: COMPLETED ·Phase: PHASE1
-
Intermittent Oral Naltrexone Enhanced With an Ecological Momentary Intervention for Methamphetamine-using MSM
NCT04791969 ·Status: COMPLETED ·Phase: PHASE2
-
Hyperalgesia in Methadone Patients: Can it be Treated?
NCT00333242 ·Status: UNKNOWN ·Phase: PHASE1
-
Comparing Opium Tincture (OT) With Methadone for Medication-assisted Treatment of Opioid Use Disorder
NCT02502175 ·Status: COMPLETED ·Phase: PHASE3
-
Transdermal Patch for BupRenorphine Induction DurinG PrEgnancy (Patch BRIDGE)
NCT05790252 ·Status: RECRUITING ·Phase: PHASE3
-
User Acceptability of a Device-Based Opioid Overdose Intervention
NCT04530591 ·Status: COMPLETED