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Pain, Postoperative clinical trials

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NCT ID: NCT00938821 Completed - Caudal Anesthesia Clinical Trials

Very Low Dose Caudal Morphine for Postoperative Pain Management

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

This is a chart review. The aim of this study is to investigate the effectiveness and side effects of very low dose morphine administered caudally to children that went to surgical procedures that used caudal anesthesia. The study compares caudal block with Bupivacaine (1 ml kg_1 of bupivacaine 0.25% and saline 0.02 ml kg_10) with very low dose morphine (a mix of 1 ml kg_-1 of ropivacaine 0.2% and preservative-free morphine: 10 µg kg-1).

NCT ID: NCT00938548 Completed - Pain, Postoperative Clinical Trials

Perioperative Administration of Pregabalin for Pain After Mastectomy

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

The investigators hypothesize that pregabalin will decrease post-operative pain scores and analgesic use following total mastectomy compared to placebo. The primary outcome will be acute postoperative pain, measured by a verbal numerical rating score (VNRS) and total analgesic consumption during postoperative 48 hours. The secondary outcome will be VNRS at 1 week and 1 month after operation.

NCT ID: NCT00935116 Not yet recruiting - Acute Pain Clinical Trials

Etoricoxib for Postoperative Pain After Thyroid Surgery

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

The purpose of the study is evaluate the analgesic efficacy and safety profile of the Cox-2 specific analgesic Etoricoxib (arcoxia®) when administrated pre and postoperatively for controlling pain in adult patients undergoing thyroid surgery. Patients will be followed up in the immediate postoperative period, during the first postoperative (POD) day and in POD 2, 3 and 7. It is expected that with the addition of Etoricoxib, patients will experience less pain during the overall postoperative period and also a better quality of recovery when compared with the traditional analgesic regimen.

NCT ID: NCT00927888 Completed - Pain, Postoperative Clinical Trials

Postoperative Pain and Functional Patient Outcomes After Functional Endoscopic Sinus Surgery

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

The aim of the study is to quantify postoperative pain after functional endoscopic sinus surgery (FESS) and investigate whether preemptive analgesia may positively impact intraoperative anesthetic management, decrease patient postoperative pain and discomfort, and improve patient functional outcomes.

NCT ID: NCT00927225 Completed - Pain, Postoperative Clinical Trials

Local Infiltration Analgesia in Bilateral Knee Arthroplasty - Efficacy of Subcutaneous Wound Infiltration With Local Anesthetic

Start date: September 2008
Phase: Phase 4
Study type: Interventional

Local infiltration analgesia is effective in total knee arthroplasty for postoperative pain management, but the efficacy of subcutaneous wound infiltration has not been evaluated. This study aims at evaluating the efficacy of subcutaneous wound infiltration in total knee arthroplasty in 16 patients undergoing bilateral knee arthroplasty.

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: NCT00922142 Completed - Cesarean Clinical Trials

Cesarean Postoperative Pain Satisfaction

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

Hypothesis: There is no significant difference in Cesarean patients' perceptions of overall pain management satisfaction between methods used for postoperative pain management.

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: NCT00921700 Completed - Pain, Postoperative Clinical Trials

Analgesic Effect of Paracetamol, Paracetamol + Codeine, Ibuprofen and Their Combination

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

The purpose of this study is to determine whether the combination of paracetamol (acetaminophen) and other NSAIDs with or without weak opioids can give synergistic analgesic effect.

NCT ID: NCT00921479 Recruiting - Pain, Postoperative Clinical Trials

Postoperative Course Following Wisdom Tooth Surgery

Start date: June 2005
Phase:
Study type: Observational

The purpose of this study is to determine how quality of life changes after surgical removal of wisdom teeth