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Pain clinical trials

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NCT ID: NCT02916927 Completed - Pain Clinical Trials

Intravenous Sub-dissociative Dose Ketamine Injection Versus Infusion for Analgesia in the Emergency Department

Start date: September 2016
Phase: Phase 4
Study type: Interventional

Objective: The purpose of this study is to determine if administering ketamine as an intravenous (IV) infusion over 15 minutes, as compared to an IV push, will decrease adverse drug reactions without attenuating its analgesic effects. Study design: prospective, randomized, controlled, double-blind trial.

NCT ID: NCT02915978 Completed - Pain Clinical Trials

Fentanyl Sublingual Spray for the Treatment of Moderate to Severe Post-Operative Pain

Start date: December 2016
Phase: Phase 2
Study type: Interventional

The primary objective of this trial is to evaluate analgesic efficacy of Fentanyl Sublingual Spray compared with placebo in participants with postoperative pain after a bunionectomy.

NCT ID: NCT02913833 Completed - Pain Clinical Trials

The Impact of Pain Assessment on the Hospital Length of Stay of Patients in a Rehabilitation Unit

Start date: March 9, 2016
Phase: N/A
Study type: Interventional

The financing of the Belgian hospitals is based on a system taking into account the length of hospitalization of a given patient according to his/her pathology, his/her age and his/her geriatric characteristics. This system encourages all hospital to lower the hospitalization duration to the national average for these criteria. This results in better efficiency in the management of hospitalizations but also means a swifter transfer to structures exempted from this system such as revalidation units, nursing homes and psychiatric units. An assessment of the differences in the medical practice, in terms of quality and outcomes of care, is essential for any reform willing to reduce medical costs. Pain management is part of the quality indicators within hospitals. Pain is defined by the International Association for the Study of Pain as "an unpleasant sensory and emotional experience, associated to present or potential tissue damage, or described in terms of such a damage". Several studies have showed that pain affects the quality of life and impacts the daily activities. Acute or chronic pain can cause adverse symptoms such as sleep disturbance, appetite loss, decreased concentration, mood changes and the disruption of familial, work and social activities. Pain might also slow down revalidation processes. A study performed by Aprile et al showed that pain negatively influenced the rehabilitation program of a quarter of the patients having had a stroke. The functional recovery was slower and the costs were higher. The aim of this study is to determine if the systematic evaluation of the pain of a patient hospitalized in a revalidation unit has an impact on his/her length of stay.

NCT ID: NCT02913027 Completed - Pain Clinical Trials

Can We Improve the Comfort of Pelvic Exams?

Start date: September 5, 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate patients self-reported comfort levels during each section of the pelvic exam.

NCT ID: NCT02912195 Completed - Pain Clinical Trials

Intravenous Lidocaine Versus Morphine for Severe Pain in the ED

Start date: March 2016
Phase: Phase 4
Study type: Interventional

Objective: Evaluate the analgesic efficacy of intravenous (IV) lidocaine versus provider chosen dose of IV morphine for the treatment of severe pain in the emergency department. Study design: Open-label, randomized controlled pilot study.

NCT ID: NCT02903238 Completed - Pain Clinical Trials

Brain Morphometry in OA Patients Treated With Duloxetine

Start date: July 2011
Phase: N/A
Study type: Interventional

This is a two week,single-blind study evaluating pain response and changes in brain imaging upon treatment with placebo in people with knee OA.

NCT ID: NCT02902770 Completed - Pain Clinical Trials

Intravenous Lidocaine and Ketorolac for Pain Management

Start date: October 2016
Phase: Phase 4
Study type: Interventional

The literature regarding analgesic modalities, their combinations and routes of administrations for patients with pain related to renal colic is expanding. NSAID's (IV ketorolac) and opioids (morphine) constitutes the mainstay of treatment of renal colic either alone or in combinations. Despite their synergism and analgesic superiority when administered together, both classes of these medications possess a set of unfavorable side effects that limit their use. Emerging data of the use of IV lidocaine for patients with renal colic demonstrated good analgesic efficacy and safety profile. However, none of the trials directly compared lidocaine to ketorolac or the combination of both as viable options in patients unable to tolerate or to have serious contraindications to opioids. We designed a double-blinded, randomized, controlled trial to evaluate analgesic efficacy, safety and feasibility of non-opioid analgesics and their combinations in patients with renal colic. The hypothesis and proposed study will try to determine if a combination of IV lidocaine and reduced dose of IV ketorolac is superior to either drug alone and if this non-opioid analgesic modality is effective for controlling pain of renal colic origin.

NCT ID: NCT02902627 Completed - Pain Clinical Trials

Pain in Oncolgy: Evaluation of a Non Invasive Monitoring Device (ANI). A Monocentric Prospective Study

ANIONCO
Start date: August 2012
Phase: N/A
Study type: Interventional

l'ANI (Analgesia Nociception Index The main objective of the research is to estimate the Analgesia Nociception Index (ANI) as a parameter giving the possibility of measuring the pain in painful metastatic cancer. The parameter ANI is compared with visual analogical scale (VAS) score.

NCT ID: NCT02902315 Completed - Pain Clinical Trials

Antioxidants Combined With Cryotherapy on Inflammatory Response After Resistance Exercise in Untrained Volunteers

Start date: January 4, 2017
Phase: N/A
Study type: Interventional

Acutely resistance exercise induces inflammatory responses and leukocytosis arising of oxidative stress, that clinically manifested by pain and/or delayed onset muscle soreness (DOMS). Beginners in resistance exercise programs are more vulnerable to the effects of oxidative stress as they exhibit lower antioxidant capacity, greater lipid peroxidation and present increased perception of pain after exercises that may lead to abandonment the exercises practice. Vitamins C and E are exogenous antioxidants which are able to prevent damages caused by oxidative stress. Cryotherapy decreases temperature and reduced generation of reactive oxygen species. The aim of the present research are to investigate the effects of the concomitant of vitamins and of cryotherapy on leukocytosis, inflammatory markers, oxidative stress parameters and pain in untrained individuals submitted to a resistance exercise session.

NCT ID: NCT02901275 Completed - Pain Clinical Trials

Enhancing Medication-based Analgesia in Humans

Start date: December 2016
Phase: Phase 2
Study type: Interventional

This is a single-group, within-subject, double-blind, double-dummy, placebo and active-controlled study evaluated whether the FDA-approved cannabinoid dronabinol (Marinol) would enhance analgesia, subjective reports, and cognitive performance when compared to the FDA-approved opioid hydromorphone (Dilaudid).