Clinical Trials Logo

Acute Pain clinical trials

View clinical trials related to Acute Pain.

Filter by:

NCT ID: NCT01433588 Completed - Acute Pain Clinical Trials

The Calmer Project

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

The purpose of this study is to see if the Calmer is more effective at managing acute pain in preterm infants in the neonatal intensive care than the current standard of care in the unit. Hypothesis: While receiving treatment with Calmer, infants will show lower behavioral pain scores and lower heart rates, and more stable autonomic regulation as measured by heart rate variability indices, than infants given a soother plus facilitated tucking (standard of care) during routine blood collection.

NCT ID: NCT01420159 Completed - Clinical trials for Acute Pain Due to Trauma

Efficacy and Safety of Methoxyflurane (Penthrox) for the Treatment of Acute Pain in Minor Trauma

STOP!
Start date: August 2011
Phase: Phase 3
Study type: Interventional

This study investigates the treatment of acute pain, an unpleasant feeling caused by an injury. The overall purpose of the study is to gain more information that the pain relief medicine Penthrox(Methoxyflurane) administered using the Penthrox Inhaler(a distinctive green, whistle like object that you breathe through) is safe and works at relieving pain in patients aged 12 years and older who are admitted to a hospital Emergency Department with a minor injury (known as trauma).

NCT ID: NCT01402375 Completed - Clinical trials for Analgesia After ED Discharge for Extremity Injuries

Comparing the Efficacy of Oral Opioids for Outpatient Acute Pain Management After ED Discharge Discharge

Start date: January 2012
Phase: Phase 3
Study type: Interventional

There will be 3 randomized, double-blinded clinical trials to help determine which of commonly prescribed oral opioid combination is most effective in managing acute extremity pain after discharge from the adult emergency department. The first trial compares hydrocodone 5mg / acetaminophen 500mg to codeine 30mg/acetaminophen 300mg. The second trial compares oxycodone 5mg/acetaminophen 325mg to codeine 30mg/acetaminophen 300mg. The third trial compares oxycodone 5mg/acetaminophen 325 mg to hydrocodone 5mg/acetaminophen 325 mg.

NCT ID: NCT01387750 Completed - Pain Clinical Trials

Mentholated Cream Containing Oxygenated Glycerol Triesters on Acute Pain of the Muscles and Joints

Start date: May 2007
Phase: Phase 1/Phase 2
Study type: Interventional

A single center trial to evaluate the efficacy, tolerance, and acceptability of Oxygenated Glycerol Triesters (OGT) mentholated cream on acute musculoskeletal pain in normal healthy adult volunteers suffering from a recent inflammation of muscles and joints. Patient who met eligibility requirements were instructed to identify one area on their body where they were experiencing the most acute musculoskeletal pain/discomfort. Patients were provided with visual analog scales in order to quantify their pain. Patients either received mentholated cream with or without OGT and instructed to rub on the identified site 3 times a day for 7 days. Pain and other observations were written in a diary for each day.

NCT ID: NCT01356745 Completed - Acute Pain Clinical Trials

Efficacy of Premixed Nitrous Oxide and Oxygen in Patient With Out-of-hospital Moderate Acute Pain

MEOPA
Start date: February 2010
Phase: Phase 4
Study type: Interventional

Less than 10% of patients with a traumatic pain have been managed by a physician before to be admitted in an emergency service. 50 % of those patients have been carried by paramedics. Premixed nitrous oxide and oxygen is often used by paramedics, but no scientific studies have demonstrated its efficacy. The aim of the study is to demonstrate the efficacy of premixed nitrous oxide and oxygen in patients with out-of-hospital moderate acute pain.

NCT ID: NCT01333722 Completed - Pain Clinical Trials

Acute Pain Study Following Bunionectomy

Start date: April 2011
Phase: Phase 2
Study type: Interventional

The primary purpose of this study was to evaluate analgesic efficacy and safety of hydrocodone/acetaminophen extended release compared to placebo in the treatment of moderate to severe pain following bunionectomy.

NCT ID: NCT01322074 Completed - Clinical trials for Systemic Inflammatory Response Syndrome

Systemic Inflammation Versus Acute Pain in Total Knee Arthroplasty (TKA)

Start date: August 2009
Phase: N/A
Study type: Observational

In this study we evaluate if there is a correlation between acute pain and systemic inflammatory markers after total Knee Arthroplasty (TKA).

NCT ID: NCT01311895 Completed - Acute Pain Clinical Trials

Clinical Trial Comparing Two Protocols Using Intravenous (IV) Hydromorphone

Start date: January 2011
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare two opioid protocols ("H2O" and "1+1") for the treatment of acute severe pain in the emergency department. The investigators primary hypothesis is that the "H2O" protocol will be more efficacious than the "1+1" protocol in Emergency Department patients aged 21-64 years. The primary outcome is the proportion of patients in each arm who choose to forgo additional pain medication at 60 minutes.

NCT ID: NCT01298297 Completed - Acute Pain Clinical Trials

Efficacy of Buprenorphine for Treatment of Acute Pain

Start date: February 2010
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether sublingual buprenorphine is effective in the treatment of acute pain in adult patients with extremity bone fractures

NCT ID: NCT01172730 Completed - Acute Pain Clinical Trials

The Use of Ultrasound to Measure Depth of Thoracic Epidural Space

Start date: May 2010
Phase: N/A
Study type: Observational

The purpose of the study is to evaluate the use of ultrasound scanning of the thoracic spine to define the point of insertion and the depth of the epidural space compared to the blind technique. The study hypothesis is the use of Ultrasound will improve the success rate of epidural placement and may also decrease the rate of complications.