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Opioid Use clinical trials

View clinical trials related to Opioid Use.

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NCT ID: NCT03858231 Recruiting - Pain, Postoperative Clinical Trials

Opioids Versus Non-Opioids Postoperative After Knee Arthroscopic Surgery

Start date: October 29, 2018
Phase: Phase 4
Study type: Interventional

The purpose of this study is to look at pain management with opioids versus non-opioids after knee arthroscopy. This study will determine 1) whether the most commonly used non-narcotic medications provide pain relief comparable with the most commonly prescribed narcotic medications in patients undergoing arthroscopic knee surgery, and 2) whether patients' characteristics (gender, pre-operative knee symptoms, workers compensation status and employment status) affect pain level following surgery or medication usage.

NCT ID: NCT03825471 Recruiting - Opioid Use Clinical Trials

Cranial Electrotherapy Stimulation on Anesthetics Consumption and Postoperative Pain

Start date: January 14, 2019
Phase: N/A
Study type: Interventional

Cranial electrotherapy stimulation (CES) is a non-invasive intervention to treat anxiety, depression, insomnia, and pain. But clinical studies and applications of CES in relation to acute postoperative pain are few. tThe investigators investigate a double-blind, randomized controlled trial to figure out if intraoperative CES could decrease dosage of intraoperative anesthetics and patient-controlled analgesia (PCA) consumption in patients undergoing colon cancer surgery.

NCT ID: NCT03823534 Recruiting - Pain Clinical Trials

Post-Op Pain Control for Prophylactic Intramedullary Nailing.

Start date: February 20, 2019
Phase: Phase 3
Study type: Interventional

Nationally, the opioid crisis has become a major epidemic with increasing mortality rates each year. Orthopedic surgeons routinely prescribe narcotics instead of NSAIDs for post-op pain control because of risk of delayed healing and nonunion due to NSAID use. Orthopedic oncology, however, has a unique subset of patients that undergo prophylactic placement of intramedullary femoral nails. Because no fracture is present, these patients do not rely on inflammatory healing factors, allowing for post-op NSAID use. This study sets out to determine the effect of post-op toradol use in addition to opioids compared to solely opioids in patients undergoing prophylactic nailing of the femur.

NCT ID: NCT03784573 Recruiting - Anxiety Clinical Trials

Canine-Assisted Anxiety Reduction In Emergency Care

CANINE III
Start date: January 7, 2019
Phase: N/A
Study type: Interventional

Compare the effect of a single exposure to a therapy dog and handler within the pediatric emergency department patient with anxiety by measuring the change in patient perception of anxiety before and after dog exposure using the FACES scale. We will also measure galvanic skin response (resistance to electrical current).

NCT ID: NCT03749811 Recruiting - Opioid Use Clinical Trials

Pupillometry-guided Remifentanil Infusion Versus Conventional Administration in Children

PURFT
Start date: December 4, 2018
Phase: N/A
Study type: Interventional

Our study aims to compare the total intravenous dose of remifentanil per anesthesia hour and body weight in two groups of pediatric surgical patients - an interventional group with remifentanil infusion under pupillometry monitoring, and control group without pupillometry - to figure out whether pupillometry monitoring may reduce remifentanil consumption during anesthesia while providing sufficient analgesia for surgical noxious stimuli.

NCT ID: NCT03675386 Recruiting - Chronic Pain Clinical Trials

Reducing Opioid Use for Chronic Pain Patients Following Surgery

RECOUP
Start date: September 24, 2018
Phase: N/A
Study type: Interventional

Patients with chronic pain are often prescribed long-term opioid therapy, despite the serious risks and growing concerns related to opioid use. The Toronto General Hospital has created the world's first multidisciplinary perioperative Transitional Pain Service Program (TPSP) aimed at reducing the incidence and severity of chronic post-surgical pain. The TPSP incorporates a variety of mechanisms and interventions to help patients manage pain and to wean off opioids. The approach consists of: pain education, Acceptance and Commitment Therapy (ACT), and an e-mobile self- management tool to help patients manage chronic pain more effectively. With the TPSP team, the investigators hope to continually assist patients to achieve a balance between the benefits and potential harms of opioid use to promote long-term health and well-being.

NCT ID: NCT03616236 Recruiting - Opioid Use Clinical Trials

Buprenorphine for Probationers and Parolees: Bridging the Gap Into Treatment

Start date: July 1, 2022
Phase: Phase 3
Study type: Interventional

This five-year study will evaluate the effectiveness of the administration of buprenorphine bridge treatment (BBT) to probationers and parolees compared to treatment as usual (TAU), which consists of referral to a community buprenorphine treatment program.

NCT ID: NCT03596424 Recruiting - Postoperative Pain Clinical Trials

Dexmedetomidine and Ketamine in VATS Surgery

Start date: February 1, 2018
Phase: N/A
Study type: Interventional

Postoperative pain after VATS surgery is significant and associated with moderate to high post operative morphine requirements, which can cause opioid related side effects and delay postoperative recovery. To reduce this requirement, multimodal analgesia with non opioid medication such as dexmedetomidine and ketamine can be used. These drugs have demonstrated significant opioid-sparing properties after various types of surgeries. However, very little is known about their ability to do so in VATS surgery. Also, their relative opioid-sparing properties have not been compared, and it is not known whether their combined use can lead to an additional opioid-sparing effect. The primary goal of this study will be to determine the impact of a combined intra operative infusion of ketamine and dexmedetomidine on postoperative morphine requirements in patients undergoing elective VATS, compared to both these drugs infused separately. The hypothesis is that this combined infusion will lead to a 30% further reduction in morphine requirements, 24h after surgery, compared to both these drugs infused separately.

NCT ID: NCT03418636 Recruiting - Hepatitis C Clinical Trials

The Staying Safe Intervention

Ssafe
Start date: January 31, 2018
Phase: N/A
Study type: Interventional

The growing population of young people who inject drugs (PWID) is at extremely high risk for HCV infection through the use of contaminated injection equipment, yet, to date, no behavioral intervention has been sufficiently potent to produce significant reductions in HCV incidence among PWID. To address this critical public health need, our team developed Staying Safe (Ssafe), an innovative, strengths-based, socio-behavioral HCV prevention intervention found in preliminary research to be highly acceptable and feasible, with strong indications of efficacy. The proposed randomized, controlled trial will assess the effectiveness of the Ssafe intervention in reducing both injection-related HCV/HIV risk behavior and HCV incidence among young adults (ages 18-29) who inject opioids (heroin and/or prescription opioids).

NCT ID: NCT03412448 Recruiting - Chronic Pain Clinical Trials

The Prevalence of Chronic Pain and Continued Opioid Use After Cardiac Surgery

Doul-Card
Start date: June 1, 2017
Phase: N/A
Study type: Observational

The authors propose to evaluate the prevalence of chronic post-operative pain (CPOP) and continued opioid use in the population that has undergone cardiac surgery at the Montreal Heart Institute. In addition, the authors wish to evaluate the presence of known risk factors for CPOP in this population.