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Opioid Use, Unspecified clinical trials

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NCT ID: NCT02299024 Completed - Clinical trials for Opioid Use, Unspecified

Prescribing Opioid Pain Relievers in the Emergency Department: Understanding and Optimizing the Encounter

Start date: October 2012
Phase: N/A
Study type: Interventional

The investigators overall study objective is to improve patients knowledge and safe use of opioid pain relievers upon discharge from the Emergency Department.

NCT ID: NCT02282306 Completed - Clinical trials for Opioid-related Disorders

Phone Interview to Prevent Recurring Opioid Overdoses

TTIP-PRO
Start date: September 2014
Phase: N/A
Study type: Interventional

There has been a dramatic rise in opioid overdose (OOD) deaths in recent years. Attempts to ameliorate the problem have largely focused on increasing the accessibility of naloxone, an opioid antagonist that is effective in OOD reversal. Individuals who have experienced a non-fatal OOD are at risk for additional overdoses and yet there are no interventions that specifically target this high-risk population. To address this gap, the investigators have developed the "Tailored Telephone Intervention delivered by Peers to Prevent Recurring Opioid Overdoses" (TTIP-PRO). The overall goal of the present study is to conduct a pilot evaluation of the TTIP-PRO. The research literature suggests the need for an intervention targeting patients experiencing a non-fatal OOD.

NCT ID: NCT02244099 Completed - Anxiety Clinical Trials

Controlled Substance Treatment Agreements in an Internal Medicine Residents' Clinic

Start date: September 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to characterize and improve controlled substance, carisoprodol and tramadol use in an internal medicine residents' clinic. Specific objectives of this study include: - To measure the adherence to a controlled substance treatment agreement (CSTA) before and after implementation of a population management intervention - To determine the number of patients on a CSTA with a discrepancy identified on a urine drug screen or an Ohio Automated Rx Reporting System (OARRS) report - To track the number of patients on a morphine equivalent dose (MED) of ≥ 80 mg/day before and after implementation of a review intervention - To characterize the healthcare utilization of patients taking controlled substances, carisoprodol, or tramadol by tracking the mean number of ED visits, hospital admissions, telephone calls, and clinic office visits during a 6 month period

NCT ID: NCT01313247 Not yet recruiting - Advanced Cancer Clinical Trials

Paracetamol for Cancer Pain

Start date: April 2011
Phase: Phase 4
Study type: Interventional

Randomised, double-blind placebo controlled cross-over trial Main goal: Optimize the medical pain treatment for patients with advanced cancer disease Study goal: Measure paracetamol's additional analgesic effect in a situation where the patient is concomitantly treated with oral opioids eqv. morphine > 100 mg/d.