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Postoperative Pain clinical trials

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NCT ID: NCT00974350 Completed - Surgery Clinical Trials

A Safety and Efficacy Study of SABER®-Bupivacaine for Pain Following Hernia Repair

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

This is a research study testing SABER-Bupivacaine (an experimental pain-relieving medication). SABER-Bupivacaine is designed to continuously deliver bupivacaine, a common local anesthetic, for a few days in order to treat local post-surgical pain. This study is testing SABER-Bupivacaine in people having surgery to repair a hernia. The purpose of the study is to measure and compare the safety (side effects), tolerability (ability to tolerate), and efficacy (how well it works) of two different volumes of SABER-Bupivacaine with SABER-Placebo.

NCT ID: NCT00968903 Completed - Postoperative Pain Clinical Trials

Effects of Methylprednisolone After Total Hip Arthroplasty

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

The purpose of the study is to compare the effects of pre-operative methylprednisolone (125mg iv) versus placebo on postoperative outcome after hip arthroplasty. The hypothesis is that pre-operative methylprednisolone (125mg iv) will reduce time to fulfill discharge criteria.

NCT ID: NCT00968578 Completed - Postoperative Pain Clinical Trials

Effects of Methylprednisolone After Total Knee Arthroplasty

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

The purpose of the study is to compare the effects of pre-operative methylprednisolone (125mg iv) versus placebo on postoperative outcome after knee arthroplasty. The hypothesis is that pre-operative methylprednisolone (125mg iv) will reduce pain and improve outcome.

NCT ID: NCT00964639 Completed - Postoperative Pain Clinical Trials

Postoperative Pain in Children With Cerebral Palsy After Pelvic and Femoral Osteotomies

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

This study is a comparison of postoperative pain in children with cerebral palsy after surgery on the hip or femur. One group is treated with p.o. (by mouth) or intravenous (i.v.) analgesia, and the other group is treated with local infiltration analgesia with Naropine. Pain is measured with r-FLACC, a pain-score validated for children with cerebral palsy.

NCT ID: NCT00957177 Completed - Postoperative Pain Clinical Trials

Analgetic Effect of Preoperative Pregabalin in Patients Undergoing Nephrectomy

PregabaNeph
Start date: April 2009
Phase: Phase 3
Study type: Interventional

Pregabalin 300mg or placebo are administered 1 hour preoperatively in patients undergoing elective nephrectomy. Postoperatively, patients receive a patient controlled analgesia device for self delivering opioids. Morphine consumption in the first 48 hours is documented. Hyperalgesia is measured by von-Frey-Filaments.

NCT ID: NCT00949429 Completed - Postoperative Pain Clinical Trials

Quality of Postoperative Pain Management in Cardiac Surgical Patients

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

The purpose of this study is to determine the incidence and risk factors of moderate to severe pain after cardiac surgery, and compare the preoperative pain expectation and postoperative pain experience in the same patient.

NCT ID: NCT00942565 Completed - Postoperative Pain Clinical Trials

Adjuvant Analgesic Effects of Low Dose Tramadol/Acetaminophen Combination After Open Gynaecological Surgery

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

Patient experience moderate to severe pain after abdominal surgery. This post-operative pain can also contribute to complications such as respiratory impairment, cardiovascular events, ileus, sleep deprivation and mood disturbance. Opioid based patient-controlled analgesia (PCA) is commonly employed but opioids have the side effects such as respiratory depression, nausea and vomiting, sedation, pruritus and urinary retention. Bowel motility can also be affected. Consequently alternative or adjunct analgesic medications without these side-effects have been investigated in order to reduce opioid consumption. Multimodal analgesia is a technique whereby a combination of analgesic drugs with different modes of action can be used to improve analgesia and decrease adverse effects by virtue of synergism. Postoperatively, with adjunctive analgesia, PCA morphine consumption as well as the side effects may be reduced. Non-steroidal anti-inflammatory drugs (NSAIDs) have been shown to be opioid sparing and decrease the adverse effects of PCA morphine. A recent review showed that acetaminophen combined with PCA could induce a significant opioid-sparing effect but the incidence of PCA morphine related side effects were not reduced. It is common nowadays to give oral analgesic supplements to post-operative patients on PCA morphine. Tramadol, an analogue of codeine, is one of the choices. However, some of the patients cannot tolerate the side effects such as nausea, drowsiness, sweating, postural hypotension and dry mouth. Combination of tramadol 37.5 mg and acetaminophen 375 mg, which has been used successfully to treat post-operative pain, may improve analgesic response with better tolerability. This study is to assess tramadol 37.5 mg and acetaminophen 375 mg combination on the efficacy of pain control, down stepping of morphine consumption and related adverse events with PCA use after open colorectal surgeries. Objectives: This study aims to compare and evaluate: - The efficacy of tramadol/acetaminophen combination on postoperative pain relief after lower abdominal surgeries - The effects of tramadol/acetaminophen combination on the consumption and the duration of PCA morphine use - The adverse effects related to this regimen - The effects on postoperative bowel function, tolerability of fluid and diet, ambulatory function, sleep, and duration of hospital stay - The overall satisfaction of the patients

NCT ID: NCT00925912 Completed - Postoperative Pain Clinical Trials

A Trial of Closed Hemorrhoidectomy Under Local Perianal Block Versus Spinal Anesthesia

Start date: December 2006
Phase: N/A
Study type: Interventional

Hemorrhoidectomy can be carried out under several modes of anesthesia. In western country hemorrhoidectomy usually be performed under general anesthesia, however there may be the complications resulted from general anesthesia together with associated diseases in advanced age, caudal or spinal anesthesia has been used as an alternative to general anesthesia (GA) for hemorrhoid surgery but they all require a trained anesthetist and have numerous known complications. Since, anesthesiologists are not always available then local anesthesia is an alternative mode of anesthesia that surgeon can safely carry out by their own. Local anesthetic produce a loss of sensation and muscle paralysis in a circumscribed area of body by localized effect on peripheral nerve endings. The local anesthesia is able to provide fully relaxation of the anal canal which is an ideal setting for various anal surgical procedures. The results of hemorrhoid surgery under this mode of anesthesia have been demonstrated in many publications. Local anesthesia is a safe and effective technique while fewer risks and complications compared with general or spinal anesthesia. In Thailand both spinal anesthesia and local perianal block have routinely been used for various kinds of anorectal surgery. However, so far there has no any trial conducting to compare between these two techniques.

NCT ID: NCT00921908 Completed - Postoperative Pain Clinical Trials

Multihole or Epidural Catheter for Local Anesthetic in the Wound

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

Postoperative administration of local anesthetics is effective for postoperative pain management across surgical specialties but the optimal type of catheter (single, few or multiholed catheters) has not been determined. This study investigates wound spread of a radioactive isotope (technetium) administered in different types of catheters after total hip arthroplasty.

NCT ID: NCT00895843 Completed - Postoperative Pain Clinical Trials

Protective Analgesia for Postoperative Pain Relief Following Day Case Oral Surgery

Start date: November 2006
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate whether robust analgesic regime (protective analgesia) can improve postoperative pain experience for patients undergoing lower wisdom teeth extraction under day case general anaesthetic.