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Pain clinical trials

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NCT ID: NCT02863575 Completed - Pain Clinical Trials

A Dental Pain Study Comparing The Analgesic Efficacy Of Ibuprofen/Caffeine

Start date: October 24, 2017
Phase: Phase 3
Study type: Interventional

An efficacy study assessing analgesic effect of ibuprofen/caffeine in post-surgical dental pain.

NCT ID: NCT02863081 Completed - Pain Clinical Trials

Helping Older Persons Emerge Stronger

HOPES
Start date: July 2016
Phase: N/A
Study type: Observational

Select Specialty, a national network of more than 100 LTACHs across the United States, has expressed the desire to adopt the ABCDEF bundle as a "standard of care" for its patients. As part of this initiative, Select first plans to conduct an ABCDEF bundle quality improvement project in one of its local hospitals. The overall purpose of this before-after study is to study prospectively the process and effects of implementing the ABCDEF bundle into the everyday care of patients requiring prolonged mechanical ventilation in the LTACH setting.

NCT ID: NCT02859168 Completed - Breast Cancer Clinical Trials

Myofascial Induction in Breast Cancer Survivors

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

The purpose of this study was to show the immediate effects of myofascial induction on perceived pain and anxiety, cervical/shoulder range of motion and mood state in breast cancer survivors suffering shoulder/arm morbidity.

NCT ID: NCT02857361 Completed - Pain Clinical Trials

Crossover Study to Evaluate the PK Effects of Two Different Wafer Administration Protocols.

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

The study will look at whether it is preferable to administer two wafers simultaneously or separately.

NCT ID: NCT02856087 Completed - Pain Clinical Trials

The Effect of Ultra-low-dose Naloxone on Remifentanil-induced Postoperative Hyperalgesia - A Randomized Controlled Study

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

High-dose remifentanil infused intraoperative ironically results in postoperative hyperalgesia. Ultra-low dose nalxone is demonstrated to prevent these opioid-induced hyperalgesia in animal model. In this clinical trial in patients undergoing general anesthesia with remifentanil, we evaluate the effects of ultra-low-dose naloxone on remifentanil-induced hyperalgesia

NCT ID: NCT02853591 Completed - Pain Clinical Trials

Comparison of Pneumoinsufflation Modes and Pressure Settings in Gynecology

Start date: October 2016
Phase: N/A
Study type: Interventional

This study seeks to evaluate post-operative patient pain and quality of life, and intra-operative hemodynamic status and changes in inflammatory markers, with use of a pressure-barrier insufflator and conventional insufflator at high and low pneumoperitoneum pressure settings.

NCT ID: NCT02848729 Completed - Pain Clinical Trials

Drug Interactions Between Morphine and Orally or IV Administered Acetaminophen

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

Morphine is the opioid used to treat pain after surgery. Acetaminophen (called APAP) can reduce the amount of opioids needed for this. The problem is that morphine slows down digestion. That can delay pain relief from APAP pills. It can even change what the body does to the drug [pharmacokinetics (PK)]. Some doctors have started using intravenous (IV) APAP with morphine, instead of the pills. This study will measure the PK of APAP pills and IV when used with morphine in healthy volunteers. IV APAP will likely be more effective and cause fewer side effects when used with morphine to treat pain after surgery.

NCT ID: NCT02848365 Completed - Pain Clinical Trials

Incidence and Severity of Postoperative Sore Throat And Intubation Response by Using Different Devices for Endotracheal Intubation

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

Postoperative sore throat (POST) is a common problem following the use of endotracheal intubation during general anaesthesia. It leads to dissatisfaction and discomfort after surgery and can delay a patient's return to normal routine activities. POST has been rated by patients as the eighth most adverse effect in the postoperative period. The incidence of sore throat after endotracheal intubation varies from 14.4-90%. Laryngoscopy and tracheal intubation also leads to hemodynamic stress response. The response can be deleterious in patient with or without cardiac disease. It is related to the degree of manipulation of the airway during endotracheal intubation and has been studied during intubation for some equipment used for endotracheal intubation

NCT ID: NCT02842554 Completed - Clinical trials for Painful Diabetic Neuropathy (PDN)

Training "Pain Connoisseurs" for Efficient Analgesic Proof-of-Concept Studies

Start date: August 2013
Phase: Phase 4
Study type: Interventional

The purpose of this study is to assess the ability of Evoked Pain Training (EPT) and Drug/ Placebo Administration (DPA) training to increase subjects' ability to discriminate between active and placebo treatments in a double-blind crossover trial of a known analgesic, measured by standardized effect size, relative to untrained control subjects.

NCT ID: NCT02840942 Completed - Pain Clinical Trials

Robots to Reduce Pain During IV Placement

Start date: September 1, 2016
Phase: N/A
Study type: Interventional

Peripheral intravenous catheters (IVs) are utilized in the majority of hospitalized children. The placement of IVs requires significant staff time, contributes to health care costs, and causes pain and distress in the patients receiving them. Techniques currently used at Children's Hospital Los Angeles (CHLA) to reduce children's anxiety and increase success of IV placement center depends on members of the Child Life Department distracting patients during insertion. Recent literature has suggested that humanoid robots can be a powerful form of distraction and lead to decreased pain during painful procedures in children. Work done by the University of Southern California (USC) Interaction Lab has shown that socially assistive robots can use techniques more complex than pure distraction to lead to a human-robot interaction that is perceived as more positive by the human. The investigators propose a project pairing children receiving an IV with either a (1) Child Life staff member only (2) pure distraction robot + Child Life or (3) an robot teaching coping skills + Child Life with a goal of reduced pain. Pain will be measured by participant self-report, family member perceived pain, parasympathetic activation, and pain behaviors as measured by video.