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Pain, Postoperative clinical trials

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NCT ID: NCT00221260 Completed - Clinical trials for Post Operative Pain Control

Perioperative Epidural Trial (POET) Pilot Study

Start date: September 2005
Phase: N/A
Study type: Interventional

To investigate if the use of perioperative neuraxial blockade reduces post-operative mortality and cardiorespiratory events compared to intraoperative general anesthesia AND postoperative IV narcotic analgesia. This is a feasibility study to determine if recruitment and execution of the protocol could be done in a timely manner in a much larger trial

NCT ID: NCT00210210 Completed - Breast Cancer Clinical Trials

Administration of Ketamine to Prevent the Post-operative Pain

KETAMINE
Start date: February 2004
Phase: Phase 3
Study type: Interventional

The surgery of breast cancer is responsible for post-operative pain, needing in about 30% some morphine consumption; like that, the association of ketamine with general anaesthesia may decrease morphine's use and so its adverse effects. The purpose is to evaluate the analgesic effect of a receptor NMDA's antagonist ( ketamine)

NCT ID: NCT00210158 Completed - Chronic Pain Clinical Trials

Intraoperative Nitrous Oxide and Postoperative Pain for Patients With Current Opioid Treatment

PROTOX
Start date: January 2005
Phase: N/A
Study type: Interventional

Peroperative opioids are known to induce N-Methyl-D-Aspartate dependent enhancement of postoperative hyperalgesia. For patients with current opioid treatment, these phenomena could be exagerated and could produce greater postoperative opioid consumption and higher pain score. Since Nitrous oxide has anti- N-Methyl-D-Aspartate properties, the aim of this study was to evaluate, in patients with current opioid treatment, the effects of peroperative Nitous oxide on postoperative opioid consumption and pain score, after vertebroplasty.

NCT ID: NCT00210132 Completed - Cancer Clinical Trials

Analgesic Efficacy of Inter Pleural Ropivacaine Road in Post Thoracotomy Pain for Oncologic Surgery

ROPAL 1
Start date: October 2003
Phase: Phase 2
Study type: Interventional

The purposes of this study are: 1. To determine the efficacy of inter pleural analgesia 2. To determine the plasmatic concentration of ropivacaine by inter pleural road

NCT ID: NCT00209495 Completed - Pain, Postoperative Clinical Trials

Effect of Paracetamol,Pregabalin and Dexamethasone on Pain and Opioid Requirements in Postoperative Patients

Start date: June 2005
Phase: Phase 4
Study type: Interventional

Women scheduled for abdominal hysterectomy needs postoperative pain treatment, i.e. morphine. Unfortunately morphine has side-effect: nausea, vomiting, sedation and dizziness, which is unpleasant for the patients and sometimes keeps them at bed longer time than needed. We investigate in new combinations of analgesics for postoperative pain, hoping to minimize the need for morphine.

NCT ID: NCT00199316 Unknown status - Postoperative Pain Clinical Trials

Postoperative Pain Control After Kidney Surgery : a Comparison of Intrathecal Morphine Plus PCA and PCA Only

Start date: January 2005
Phase: N/A
Study type: Interventional

postoperative pain after kidney surgery is very high. We always use PCA for postopertive pain. But almost patients still had severe pain. We try to use spinal morphine before operation aims to reduce pain.

NCT ID: NCT00188071 Completed - Abortion, Induced Clinical Trials

Postoperative Pain After Medical Abortion Under Local Anesthesia : Comparison of Several Analgesic Regimen

Start date: September 2002
Phase: N/A
Study type: Interventional

- To compare postoperative analgesia by paracetamol 1gr or ketoprofen 100 mg or the combination of these two analgesics - each treatment beeing allocated by randomization

NCT ID: NCT00186732 Completed - Pain, Postoperative Clinical Trials

Comparison of Subcuticular Suture Versus Surgical Staples for Closure of Pfannenstiel Skin Incisions

Start date: July 2005
Phase: N/A
Study type: Interventional

This study compares methods of closure for Pfannenstiel incisions commonly used during gynecological and obstetrical surgery. Patients are assigned to closure by either surgical staples or a buried suture. Information is collected on the day of surgery, post-operative day two and at the six-week follow up visit. The amount of pain and cosmetic result are compared. Infection rates will also be monitored for the two groups. The study hypothesis is as follows: subcuticular (buried) sutures as compared to surgical staples lead to decreased post-operative pain and improved cosmetic result. Infection rates are similar for both groups.

NCT ID: NCT00180687 Completed - Pain, Postoperative Clinical Trials

Clinical Trial of the Use of Intraperitoneal Local Anaesthetic

Start date: October 2004
Phase: Phase 3
Study type: Interventional

Patients undergoing keyhole gall bladder removal will be divided into 3 groups, one control, one will have local anaesthetic and the third will have normal saline nebulised into their abdomen before closure of the wounds to reduce postoperative pain. These medications will be given on top of the standard pain management protocol.

NCT ID: NCT00178178 Completed - Pain, Postoperative Clinical Trials

Arthroscopic Anterior Cruciate Ligament Reconstruction: A Comparison of Three Catheter Placement Positions

Start date: March 2005
Phase: N/A
Study type: Interventional

This investigation will evaluate the subjective effect on postoperative pain of three catheter placements in the knee: 1. intraarticular infusion only, 2. patellar tendon harvest site only, 3. both intraarticular and patellar tendon harvest site.