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Opioid Use clinical trials

View clinical trials related to Opioid Use.

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NCT ID: NCT04024397 Completed - Opioid Use Clinical Trials

A Study to Evaluate Unintended Prolonged Opioid Use

Start date: October 1, 2019
Phase:
Study type: Observational

Researchers are trying to better understand how people who are prescribed opioids for short-term use, go on to receive this type of medication on a longer-term basis.

NCT ID: NCT04017013 Completed - Pain, Postoperative Clinical Trials

Therapeutic Efficacy of Intravenous Lidocaine Infusion Compared With Epidural Analgesia for Postoperative Pain Control in Adult Patients Undergoing Major Abdominal Surgery: Non-Inferiority Clinical Trial

Start date: March 1, 2020
Phase: Phase 4
Study type: Interventional

Major abdominal surgery continues is one of the most performed surgical procedures in the world, both electively and urgently. One of the main problems of this type of intervention is postoperative pain. it is shown that it increases health costs related to longer recovery times, longer hospital stay and related complications such as the increased risk of presenting chronic POP pain, which it has been estimated up to 20%, much higher if the surgery involves surgery in the gastrointestinal system. The goal of analgesia in the postoperative setting is precisely to provide comfort to patients, minimize adverse effects and complications arising from the procedure. The epidural analgesic technique (has been proposed as an analgesic management standard, since multiple studies have shown that it reduces opioid consumption, improves recovery and is a useful strategy for pain control. However, it is an invasive technique, with risk of complications such as hematomas and epidural abscesses, and it may be difficult to perform. Currently it has been shown in multiple studies that the intravenous infusion of a local anesthetic, such as lidocaine, in this type of surgical scenarios can reduce the intensity of pain, opioid consumption, hospital stay and ileus with few adverse effects. In addition, these studies propose that, being a less invasive technique, it could be easier to implement and even be safer than the epidural technique. The main hypothesis of this study is precisely that the infusion of lidocaine may be non-inferior to epidural analgesia in the analgesic management of patients undergoing major abdominal surgery.

NCT ID: NCT04015908 Completed - Opioid Use Clinical Trials

A Multimodal Analgesia Protocol Adapted for Ambulatory Surgery

Start date: August 1, 2019
Phase: Phase 4
Study type: Interventional

The primary objective of this trial is to determine whether the combination of three non-opioid analgesics (multimodal analgesia) can significantly reduce or eliminate the need for opioids after ambulatory surgery. A secondary objective would be to present credible data for insurance providers about the opioid sparing effect of these medications. This data may encourage insurance providers to support payment for short term use of certain analgesics that currently require prior authorization.

NCT ID: NCT04011176 Completed - Pain Clinical Trials

Microcurrent Treatment for Chronic Debilitating Pain

Start date: December 9, 2019
Phase: N/A
Study type: Interventional

To compare the efficacy of standard pain treatment and placebo (a microcurrent faux treatment) as opposed to standard pain treatment and microcurrent therapy in any primary care patients over a three month period.

NCT ID: NCT04010266 Completed - Pain, Postoperative Clinical Trials

RelieVRx for Total Knee Arthroplasty (TKA) for the Reduction of Acute Postoperative Pain and Opioid Use

Start date: March 1, 2021
Phase: N/A
Study type: Interventional

This is a single-center, prospective, randomized, controlled study of the appliedVR RelieVRx headset in subjects undergoing Total Knee Arthroplasty (TKA). This study will evaluate two primary endpoints - effectiveness of a single use of RelieVRx in the reduction of acute postoperative pain by 20%; and overall effectiveness of RelieVRx as an opioid-sparing intervention, where opioid consumption is reduced by at least 20% over a 90-day postoperative period in the interventional, standard of care (SOC) plus RelieVRx group compared to the control, SOC group.

NCT ID: NCT04005599 Completed - Postoperative Pain Clinical Trials

Opioid Sparing General Venous Anesthesia With Magnesium Sulfate

Start date: June 3, 2019
Phase: N/A
Study type: Interventional

Magnesium sulfate has been shown to be useful in many situations in medicine, such as eclampsia prevention and treatment, pulmonary hypertension, arterial pressure, asthma, cardiac arrhythmias and pheochromocytoma. Recently there has been a growing a big interest in this drug as an useful adjuvant in anesthesia, with analgesic and anesthetic sparing effect, antihyperalgesic property and potentialization of the neuromuscular blocker agent effect. On the other hand there has been a growing concern related to opioid administration, such as hyperalgesia, delayed return of intestinal function and the (still controversial) possibility of facilitating effect on tumor growth and metastases in cancer patients. This project is based on a previous randomized, double blind prospective trial (conducted by one of these authors and not yet published) comparing two groups of patients who received general intravenous total anesthesia with propofol in controlled target infusion. The surgical stress index is obtained by the interaction between the interval between heart beats and the amplitude of the photoplethysmography wave, whose algorithm generates a number related to the hemodynamic result of the increase of the sympathetic tone, which has shown to be the most sensitive resource in detecting the imbalance between the stimulus nociceptive and anti-nociception.

NCT ID: NCT03999450 Completed - Opioid Use Clinical Trials

Preventing Premature Death in Patients With Serious Opioid-related Infection

Start date: October 8, 2019
Phase: N/A
Study type: Interventional

The purpose of this study is to test the efficacy of a combination of motivational interventions and a brief therapy session to increase the adherence to medication-assisted treatment (MAT) for opioids.

NCT ID: NCT03991546 Completed - Pain, Postoperative Clinical Trials

Pain and Narcotic Usage After Orthopaedic Surgery

Start date: June 3, 2016
Phase: N/A
Study type: Interventional

This study aims to 1) observe the course of pain, 2) utilization of opioid pain medication, and 3) possible effect of a behavioral intervention delivered via an automated mobile phone messaging robot in patients undergoing surgical treatment of a traumatic orthopaedic injury.

NCT ID: NCT03986866 Completed - Opioid Use Clinical Trials

Video-based, Patient-Focused Opioid Education in the Perioperative Period

Start date: April 29, 2019
Phase: N/A
Study type: Interventional

This is a pilot study designed to assess the feasibility of using a novel, video-based opioid education tool for opioid naïve ambulatory surgery patients in the perioperative period.

NCT ID: NCT03961152 Completed - Pain Clinical Trials

Effect of the PainCoach App on Pain and Opiate Use After Total Knee Replacement

Start date: January 15, 2016
Phase: N/A
Study type: Interventional

Less is known about pain and opiate use at home directly after total knee replacement (TKR). Regarding side effects, low opiate use is desired. An e-health application, PainCoach app, was developed to guide patients in pain control and opiate use. The aim of this study was to investigate the effect of the PainCoach app on pain and opiate use in TKR patients in the first two weeks at home after surgery. The hypothesis was that the use of this app would decrease pain and opiate use.