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Pain clinical trials

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NCT ID: NCT01561547 Completed - Pain Clinical Trials

Trial of Repeated Analgesia With Kangaroo Care

TRAKC
Start date: June 2012
Phase: Phase 3
Study type: Interventional

Mothers can provide pain relief to their newborns, even in the context of intensive neonatal care. There is a recent accumulation of data, being analyzed by ourselves in a Cochrane review, that mothers holding their infants in a bare-chested skin-to-skin position, known as Kangaroo Mother Care (KMC), is effective in diminishing pain response during a single painful procedure. While evidence is compelling, leading to recommendations for its use, to date there is not a single study on the repeated efficacy to reduce pain. Current guidelines recommend sweet taste for minor painful procedures. Although there is some controversy about its continued use in this population based on one study with negative neurodevelopmental outcomes as well as its potential interaction with dopaminergic development, oral sucrose (sweet taste) remains efficacious in decreasing pain response over several weeks. The combination of KMC and sucrose is marginally more potent, but again, long term use remains unstudied. AIMS. To test the repeated efficacy in diminishing pain from heel lance of KMC compared to usual care (sucrose), and of KMC in combination with sucrose by examining each condition at least three times during NICU stay. A secondary aim is to compare these interventions on neurodevelopment at discharge from the NICU.

NCT ID: NCT01559701 Completed - Pain Clinical Trials

Long-term Safety of PF-00345439 (Oxycodone)

Start date: April 2006
Phase: Phase 3
Study type: Interventional

Long-Term Safety Of PF-00345439 (Oxycodone) In Patients With Moderate To Severe Chronic Low Back Pain Or Osteoarthritis

NCT ID: NCT01559259 Completed - Pain Clinical Trials

Evaluation of the Efficacy of Novel Ibuprofen Acetaminophen Combination Formulations in the Treatment of Post-surgical Dental Pain

Start date: April 10, 2012
Phase: Phase 2
Study type: Interventional

This study will determine the overall analgesic efficacy of three different fixed dose ibuprofen plus acetaminophen formulations compared to ibuprofen alone and to placebo.

NCT ID: NCT01555476 Completed - Pain Clinical Trials

Study to Test the Blood to See if a New Medicine is Likely to Provide Pain Relief Similar to a Product Already Sold in Stores

Start date: February 2012
Phase: Phase 1
Study type: Interventional

This study is designed to assess bioequivalence between one test and one reference formulation used for temporary relief of pain. The results will help decide if the new medicine is likely to provide pain relief similar to the product being sold.

NCT ID: NCT01553578 Completed - Pain Clinical Trials

Healing Touch or Guided Imagery In Treating Pain, Fatigue, Nausea, and Anxiety in Patients Undergoing Chemotherapy

Start date: February 2012
Phase: N/A
Study type: Interventional

This randomized clinical trial studies healing touch or guided imagery in treating pain, fatigue, nausea, and anxiety in patients undergoing chemotherapy. Healing touch and guided imagery may help treat complications caused by chemotherapy. It is not yet known whether healing touch or guided imagery is more effective in treating pain, fatigue, nausea, and anxiety in patients undergoing chemotherapy

NCT ID: NCT01553253 Completed - Pain Clinical Trials

From ACute To Chronic Postoperative Pain in Patients for Elective Cholecystectomy

FACTS1
Start date: April 2010
Phase: N/A
Study type: Observational

Chronic Pain is a wellknown complication after cholecystectomy. Intensity of the pain in the first week after the operation is a predictive factor for the development of chronic pain, but it is unknown whether the risk is more related to one of the different components of acute pain (ie somatic, visceral, referred). Furthermore the chronic pain has not been systematically described in terms of type of pain or sensory abnormalities etc. (allodynia, hyperalgesia etc.). The purpose of the study is to examine whether intensity of components of acute pain is predictive for development of chronic pain after cholecystectomy and to characterize the chronic pain by quantitative sensory testing. DNA-samples are collected to examine genetical factors, important for perception of pain, and the development of chronic pain.

NCT ID: NCT01552863 Completed - Pain Clinical Trials

A Study To Characterize The Pharmacokinetics Of Oxycodone In Healthy Volunteers

Start date: March 2012
Phase: Phase 1
Study type: Interventional

This is an open-label (both the physician and healthy volunteer know which medication will be administered), single-dose, 6- dosing period study to characterize the pharmacokinetics of oxycodone (process by which oxycodone is absorbed, distributed, metabolized, and eliminated by the body). This study will consist of three parts that will take place over approximately 90 days. Part 1 of the study has 4 dosing periods, while Parts 2 and 3 have one dosing period each.

NCT ID: NCT01552850 Completed - Pain Clinical Trials

Pharmacokinetics And Relative Bioavailability Study Of Oxycodone

Start date: April 2012
Phase: Phase 1
Study type: Interventional

To estimate the pharmacokinetics and relative bioavailability of oxycodone after administration of 40 mg doses of four PF-00345439 formulations and oxycodone in solution

NCT ID: NCT01552746 Completed - Pain Clinical Trials

From ACute To Chronic Postoperative Shoulder Pain in Patients for Elective Lobectomy

FACTS2
Start date: January 2012
Phase: N/A
Study type: Observational

Shoulder pain is a well known problem after thoracical surgery. The pathogenesis of the pain is uncertain, but mainly a mix of referred pain and mechanical strain to the shoulder. It is believed to last a few days. Persisting shoulder pain after thoracical surgery is a problem 1 year after surgery, but it is unknown if it is related to acute postoperative shoulder pain. The purpose of the study is to systematically describe postoperative shoulder pain after lobectomy and examine the time progress up to 1 year after surgery.

NCT ID: NCT01551797 Completed - Pain Clinical Trials

A Pharmacokinetic Study to Compare Sustained Release and Standard Paracetamol Formulations.

Start date: May 2010
Phase: Phase 1
Study type: Interventional

This proof of principle study will evaluate an experimental formulation of paracetamol that is being developed for eventual long lasting use. This study is also used for drug safety evaluation.