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Analgesia clinical trials

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NCT ID: NCT00852046 Withdrawn - Analgesia Clinical Trials

Adjunct Dexmedetomidine (Precedex®) Therapy Impact on Sedative and Analgesic Requirement

Start date: February 2009
Phase: Phase 4
Study type: Interventional

Assess impact of increasing dose of dexmedetomidine on total daily dose of fentanyl and propofol while maintaining sedation in a mechanically ventilated patient in a general medical intensive care unit.

NCT ID: NCT00799201 Terminated - Analgesia Clinical Trials

Enteral Naloxone Versus a Traditional Bowel Regimen for the Prevention of Opioid Induced Constipation in Trauma Patients

Start date: August 2007
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine if enteral naloxone is more effective than a traditional bowel regimen in the prevention and treatment of constipation and impaired gastric motility in critically ill trauma patients.

NCT ID: NCT00791791 Completed - Analgesia Clinical Trials

Evaluation of Surgical Stress Index (SSI) During Sevoflurane/Remifentanil Anesthesia

Start date: August 2008
Phase: N/A
Study type: Interventional

The aim of the present prospective randomized study was to challenge the ability of SSI to detect painful stimulation during sevoflurane - remifentanil anesthesia.

NCT ID: NCT00791024 Completed - Analgesia Clinical Trials

Development of a New Method for Analgesia

Start date: November 2008
Phase: Phase 1/Phase 2
Study type: Interventional

Aim: To examine a new method to perform local anesthesia in order to diminish the inconvenience by the procedure in patients before performing intubation or oesophagogastroduodenoscopy.

NCT ID: NCT00789412 Completed - Pain Clinical Trials

Surgical Stress Index as a Tool for Monitoring Analgesia and/or Sedation in Critically Ill Patients

Start date: August 2008
Phase: N/A
Study type: Observational

The hypothesis of the study is: Does the Surgical Stress Index (SSI) correlate with the Behavioral Pain Scale (BPS), the Ramsay Sedation Scale (RSS)and/or the Behavioral Pain Scale(BPV) and can therefore be used to monitor the quality of analgosedation in noncommunicative intensive care unit patients?

NCT ID: NCT00782951 Terminated - Analgesia Clinical Trials

A Comparison of Analgesic Efficacy Between a Single Dose of ORG 28611, Morphine, and Placebo After Dental Impaction Surgery (Study P05800)

Start date: July 2007
Phase: Phase 2
Study type: Interventional

Patients will receive a single intravenous (IV) infusion administered over 3 minutes of either ORG 28611 (SCH 900111), 0.12 mg/kg morphine sulphate, or placebo, within 6 hours after dental surgery, when they experience moderate to severe dental pain. Patient will then be evaluated with pain assessments at Baseline, 5, 10, 15, 30, 45, 60, and 90 minutes; and 2 through 8 hours or before rescue medication is needed.

NCT ID: NCT00772187 Completed - Analgesia Clinical Trials

Intraoperative and Postoperative Analgesia for Laparoscopic Surgery.

Start date: October 2007
Phase: Phase 4
Study type: Interventional

Main Hypothesis: laparoscopic surgery is very painful to patient during and after surgery. We would like to compare different analgesic methods.

NCT ID: NCT00762554 Withdrawn - Analgesia Clinical Trials

Depodur vs Fentanyl Infusion for Post-C/S Analgesia

Start date: October 2008
Phase: N/A
Study type: Interventional

Epidurally administered Depodur provides equal or superior analgesia as an epidural infusion of fentanyl for the first 48 hours after a cesarean section.

NCT ID: NCT00761059 Recruiting - Analgesia Clinical Trials

Analgesic Efficacy of Oral Glucose in Preterm Neonates During Suctioning

Glucose FG
Start date: October 2008
Phase: N/A
Study type: Interventional

Nasopharyngeal suctioning is a painful procedure that often becomes necessary in the care of preterm infants under CPAP therapy several times a day. Since the use of analgetic and sedative drugs is accompanied with multiple side effects these are usually being avoided. Glucose 20% has been shown to have an analgesic effect when administered to preterm infants previous to some painful procedures (i.e blood sampling). In this clinical trial the efficacy of orally administered Glucose 20% for relieving the procedural pain of nasopharyngeal suctioning is tested. The investigators' study has a cross-over design and is to include 40 patients.

NCT ID: NCT00747292 Recruiting - Analgesia Clinical Trials

Peri-Operative Management of Patients Undergoing Laparoscopic Colorectal Surgery

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

The aim is to ascertain which method out of epidural, spinal or patient controlled analgesia (PCA) is the most appropriate in fluid optimised patients after laparoscopic colorectal surgery in terms of pain control, length of hospital stay and time for gut recovery. The second aim is to assess the physiological changes that occur when the patient is placed in steep trendelenberg position together with the creation of the pneumoperitoneum.