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Pain, Postoperative clinical trials

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NCT ID: NCT00653926 Completed - Postoperative Pain Clinical Trials

Local Infiltration Analgesia Following Unicompartmental Knee Arthroplasty

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

The primary aim of this study is to evaluate if intra- and postoperative administration of ropivacaine, ketorolac and epinephrine into the operating field would affect hospital stay. Secondary end-points are morphine consumption, pain intensity and side effects. In an attempt to assess the safety of this technique, knee function and patient satisfaction scores are assessed up to 6 months after surgery.

NCT ID: NCT00653133 Completed - Postoperative Pain Clinical Trials

Multicenter Continuous Peripheral Nerve Block Surveillance Study

cpnb
Start date: May 2007
Phase: N/A
Study type: Interventional

This two tiered study is a multi-center, open label, surveillance study of the use of continuous nerve blocks with the ON-Q® C-bloc and either nerve stimulator or ultrasound guided continuous nerve block techniques. This study was developed to investigate specific aspects of complication rates related to continuous nerve block techniques in patients undergoing orthopedic surgical procedures.

NCT ID: NCT00650598 Completed - Pain, Postoperative Clinical Trials

A Multicentre, Double-Blind, Double-Dummy, Randomised Study of the Analgesic Efficacy and Safety of Valdecoxib Compared to Diclofenac Sodium in Patients Undergoing Knee Arthroscopy for Anterior Cruciate Ligament (ACL) Reconstruction

Start date: March 2004
Phase: Phase 4
Study type: Interventional

To demonstrate non-inferiority of valdecoxib 20 mg twice daily (BID) (with an initial loading dose of 40 mg followed by a second dose of 20 mg on the first day only) with diclofenac sodium delayed release 75 mg BID in analgesic efficacy, in subjects undergoing knee arthroscopy procedure for anterior cruciate ligament (ACL) reconstruction, when administered for 6 (±1) days.

NCT ID: NCT00643032 Not yet recruiting - Post-Operative Pain Clinical Trials

Preoperative Anxiety and Postoperative Pain in Children

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

We wish to study which method of local injection of analgesic (before or during surgery) is the more effective method to reduce post-operative pain in children. In addition, we wish to study which pre-operative educational intervention is more effective in reducing anxiety in children and their family.

NCT ID: NCT00638508 Completed - Postoperative Pain Clinical Trials

ON-Q Pump Infusion of Ketorolac and Ropivacaine at the Wound Site for Postoperative Pain Management

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

After surgery it is normal to experience some pain at the site of operation. In order to reduce the pain, medication such as Morphine is injected into a vein using a Patient Controlled Analgesia (PCA) pump that is kept at bed side, and is activated by the patient when needed. However, Morphine is an opioid drug, which can cause side effects such as sedation, nausea, vomiting, and reduced breathing on prolonged use. In addition to the opioid drugs, local anesthetics, and other drugs called Non steroidal anti inflammatory drugs (NSAIDs) have been injected locally to provide prolonged pain relief without the side effects of morphine. Recently a portable device called ON-Q pump has been developed to continuously infuse the local anesthetic through 2 small catheters inserted at the wound site. The ON-Q Pump is a small tennis ball sized unit made of a soft synthetic material that slowly infuses the drug through the catheters by elastic force. This pump is very safe and is attached to a bedside pole or the patient's hospital gown. This pump has already been approved by the FDA for clinical use, and has been reported to provide effective pain management after some surgical procedures. The primary aim of the present study is to evaluate the relative efficacy of the drugs Ketorolac and Ropivacaine infused through the ON-Q pump in reducing the pain following gynecologic surgery. Ketorolac and Ropivacaine are approved drugs that are frequently used for post operative pain relief. Our hypothesis is that these two drugs in combination will provide better analgesia than Ketorolac alone.

NCT ID: NCT00638404 Terminated - Pain Clinical Trials

Severity Postoperative Pain Prediction

Start date: August 2007
Phase:
Study type: Observational

A simple preoperative evaluation assessing level of anxiety, anticipated pain, and intensity rating of audio tone will predict the severity of postoperative pain after surgery.

NCT ID: NCT00632580 Recruiting - Pain, Postoperative Clinical Trials

Intra- Versus Extraarticular Injection of Ropivacaine in Total Knee Arthroplasty

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

The purpose of this study is to evaluate the optimal site for application of local anesthetics in total knee arthroplasty surgery. The hypothesis is, that improved pain relief is obtained when administering local anesthetics in the tissues sourrounding the knee joint compared to the knee joint itself.

NCT ID: NCT00626886 Completed - Postoperative Pain Clinical Trials

Efficacy, Safety and Pharmacokinetic Profile of a Collagen Bupivacaine Implant in Men After Open Mesh Herniorrhaphy

Start date: March 11, 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether the CollaRx Bupivacaine implant is safe and effective in reducing the amount of narcotic pain medication needed to control pain during the first 24 hours after herniorrhaphy.

NCT ID: NCT00625911 Completed - Post Operative Pain Clinical Trials

Ketamine Improves Post-Thoracotomy Analgesia

Start date: September 2001
Phase: N/A
Study type: Interventional

Thoracotomy for lung tumor or for minimally invasive direct coronary artery bypass (MIDCAB) surgery, may be associated with debilitating pain. Ketamine was shown to enhance opioid antinociception and prevent opioid resistance. We hypothesize that ketamine given with morphine would lower morphine consumption and narcotic related side effects after thoracotomy and provide superior analgesia to morphine given alone.

NCT ID: NCT00624910 Completed - Postoperative Pain Clinical Trials

Efficacy and Safety of a Collagen Bupivacaine Implant in Women Following Abdominal Hysterectomy

Start date: December 27, 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether the CollaRx Bupivacaine implant is safe and effective in reducing the amount of narcotic pain medication needed to control pain during the first 24 hours after abdominal hysterectomy surgery.