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Postoperative Pain clinical trials

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NCT ID: NCT00889148 Completed - Postoperative Pain Clinical Trials

Morphine COnsumption in Joint Replacement Patients, With and Without GaBapentin Treatment, a RandomIzed ControlLEd Study

MOBILE
Start date: October 2007
Phase: N/A
Study type: Interventional

Total hip arthroplasty is amongst the most painful procedures postoperatively, and pain management can be a challenge. Different measures have been introduced to manage severe postoperative pain in these patients. Previous studies have investigated gabapentin in acute postoperative pain and demonstrated reduced postoperative pain, postoperative morphine consumption, morphine related side effects, and postoperative pain scores. To date, this analgesia adjunct has yet to be investigated for total joint arthroplasty patients.

NCT ID: NCT00886236 Completed - Postoperative Pain Clinical Trials

Study of the Effect of the Drug Gabapentin on Postoperative Pain and Incidence of Postoperative Nausea and Vomiting

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

The purpose of this research study is to evaluate the drug gabapentin (Neurontin®) for its ability to reduce postoperative pain, the need for morphine-like pain medication, and the severity and frequency of postoperative nausea and vomiting in laparoscopic gastric bypass surgery patients.

NCT ID: NCT00877266 Completed - Postoperative Pain Clinical Trials

Ultrasound Guidance Versus Electrical Stimulation for Perineural Catheter Insertion

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

This research study is to determine the relative times for perineural catheter placement with the use of ultrasound versus electrical stimulation. The perineural catheter is placed next to the nerves through which local anesthetic is placed to provide pain control following surgery. This study may determine if one method is associated with increased success rate and patient comfort.

NCT ID: NCT00876681 Completed - Postoperative Pain Clinical Trials

Ultrasound Guidance Versus Electrical Stimulation for Continuous Popliteal-Sciatic Nerve Blocks

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

Research study to determine if pain relief following foot and/or ankle surgery is influenced by the technique used to place perineural catheter. The catheters are placed using ultrasound-guidance or nerve stimulation and the method is selected at random using a computer program. This may help to determine if one of these methods is associated with an increased success rate and incidence of foot numbness during the infusion.

NCT ID: NCT00868348 Completed - Postoperative Pain Clinical Trials

A Comparison of Naropin and Ketorolac for Postoperative Analgesia After Total Knee Arthroplasty

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

The purpose of this study is to determine wether ketorolac is effective in the treatment of postoperative pain after total knee arthroplasty

NCT ID: NCT00842842 Completed - Postoperative Pain Clinical Trials

Mesh Fixation With Intraperitoneal Tisseel

MEFIXIT
Start date: August 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether mesh fixation in laparoscopic umbilical hernia repair with fibrin glue is superior to tacks in terms of postoperative pain and recovery.

NCT ID: NCT00831051 Completed - Postoperative Pain Clinical Trials

Comparison of the Efficacy and Safety of Q8003 Versus Its Individual Components in Bunionectomy Patients

Start date: December 2008
Phase: Phase 2
Study type: Interventional

This is a randomized, double-blind, multicenter, fixed dose factorial study of Q8003 12 mg/8 mg and Q8003 6 mg/4 mg versus its individual morphine sulfate and oxycodone hydrochloride components for the management of acute moderate to severe postoperative pain following bunionectomy surgery.

NCT ID: NCT00825344 Completed - Postoperative Pain Clinical Trials

Preoperative Etanercept Before Inguinal Hernia Surgery

Start date: January 2009
Phase: N/A
Study type: Interventional

Inguinal hernia repair is one of the most frequently performed operations in young men. Persistent pain after inguinal surgery represents a significant cause of disability, occurring in between 15%-35% of cases. In a majority of these patients, their groin pain persisted after a previous hernia repair. The main type of chronic postsurgical pain is neuropathic, caused by injured nerves. One of the principal components in the pathophysiology of postsurgical pain is cytokines, specifically tumor necrosis factor (TNF). In animal studies, injecting TNF inhibitors before nerve injury can reduce pain behaviors and neuropathology. Finding a way to reduce the incidence of postsurgical pain after hernia repair could enhance function, and reduce the need for opioids and other analgesics. The investigators intend to conduct the first randomized, controlled study evaluating whether preemptive administration of a tumor necrosis inhibitor can reduce postoperative pain and opioid consumption after hernia repair. This is important because the degree and intensity of postsurgical pain is a major predictor for the development of chronic postsurgical pain.

NCT ID: NCT00818493 Completed - Postoperative Pain Clinical Trials

Pilot Study of the Efficacy and Safety of Q8003 in Patients Who Have Undergone Total Knee Arthroplasty or Total Hip Arthroplasty

Start date: February 2009
Phase: Phase 2
Study type: Interventional

This is a Phase 2 3-arm, open label pilot study of the safety and efficacy of Q8003 in patients who have undergone primary unilateral total knee arthroplasty or total hip arthroplasty.

NCT ID: NCT00818363 Completed - Postoperative Pain Clinical Trials

A Safety and Effectiveness Study of SABER®-Bupivacaine for Pain Following Shoulder Surgery

Start date: December 2008
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. The purpose of this study is to investigate safety (if there are any side effects) associated with the use of SABER-Bupivacaine and how well it works in reducing pain and opioid-related side effects following shoulder surgery.