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Pain, Postoperative clinical trials

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NCT ID: NCT00533403 Completed - Pain, Postoperative Clinical Trials

MK0686 in Postsurgery Dental Pain (0686-002)

Start date: July 2004
Phase: Phase 2
Study type: Interventional

To compare the pain relieving effect of MK0686 to placebo or ibuprofen after dental surgery.

NCT ID: NCT00533247 Not yet recruiting - Postoperative Pain Clinical Trials

Arthroplasty Inflammation Prophylaxis With Celecoxib

Start date: n/a
Phase: N/A
Study type: Interventional

This double blinded, placebo controlled, study seeks to determine the efficacy of preoperative anti-inflammatory therapy on the reduction of postoperative pain in knee arthroplasty surgery. Pre-emptive use of NSAIDS has demonstrated only modest reduction in post-operative pain in previous studies. However, the short duration of dosing in those studies did not capitalized on the anti-inflammatory properties of NSAIDS. Short-term use of NSAIDS only provides pain relief and does not address inflammation. Traditional NSAIDS cannot be used preoperatively due to platelet effects. Celecoxib, however, is both an analgesic and anti-inflammatory, but does not interfere with bleeding. It can therefore be safely used before surgery. This study hypothesizes that the use of celecoxib for seven days preoperatively reduces postoperative inflammation and consequently pain. A detailed Medline search has not identified any studies into the preoperative use of an NSAID at a dosing level that achieves anti-inflammatory effects.If effective in reducing postoperative pain, this research could lead to a new understanding of the role inflammation plays in orthopedic procedures and other elective procedures and thus improve patient outcomes in the future.

NCT ID: NCT00529126 Completed - Postoperative Pain Clinical Trials

Phase 2 Dose-Ranging Study of SKY0402 for Prolonged Postoperative Analgesia in Subject Undergoing Hemorrhoidectomy

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

Phase 2 study to evaluate three dose levels of SKY0402 compared with 75 mg of bupivacaine HCl.

NCT ID: NCT00528177 Completed - Postoperative Pain Clinical Trials

Morphine vs. Oxycodone for Postoperative Pain Management

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

The purpose of this study is to determine whether oxycodone provides better analgesia compared to morphine after laparoscopic hysterectomy or myomectomy.

NCT ID: NCT00520338 Completed - Postoperative Pain Clinical Trials

Celecoxib for Reducing Morphine Requirement After Thyroid Surgery: A Randomized Controlled Trial

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

The purpose of this study is to determine whether celecoxib is effective in the treatment postoperative pain after thyroidectomy. The research hypothesis: There is a difference in postoperative morphine consumption in the first 24 hours after thyroidectomy between patients who received celecoxib or placebo.

NCT ID: NCT00519246 Completed - Pain, Postoperative Clinical Trials

Comparison of Pain Therapeutic Effects After Benign Mastectomy

COPTEAM
Start date: February 2007
Phase: Phase 4
Study type: Interventional

With the incremental trend of benign breast tumor, the surgical process of mastectomy was proceeded too much every day, especially in the Maternal Health Care Hospital, but whether the investigators can find another way to relieve the postoperative pain after such an operation is still unknown. The investigators hypothesized that the pain from the relatively small surgery may not be significant compared to different treatments, even if no drug was delivered to them. The investigators are enrolling patients who underwent mastectomy from benign breast tumor, and are observing the analgesic effects of different drugs.

NCT ID: NCT00518674 Active, not recruiting - Postoperative Pain Clinical Trials

Local Anesthetics After Total Knee Arthroplasty

Start date: January 2007
Phase: N/A
Study type: Interventional

The aim of this randomized, double-blind and placebo-controlled study is to evaluate the specific role of injection of local anesthetic into the intra- vs. extraarticular tissues after toal knee arthroplasty.

NCT ID: NCT00514878 Completed - Postoperative Pain Clinical Trials

Development of a Predictive Model for Post-Discharge Nausea and Vomiting (PDNV)

Apfel-PDNV
Start date: August 2007
Phase: N/A
Study type: Observational

The primary purpose of this prospective cohort study is to develop a simplified risk model for post-discharge nausea and vomiting (PDNV) in adult same-day surgery patients in the US that will allow clinicians to identify those patients who would benefit from prophylactic antiemetic strategies.

NCT ID: NCT00510666 Completed - Postoperative Pain Clinical Trials

Comparison of Butorphanol and Tramadol Associated Patient-Controlled Analgesia (PCA) After Hysterectomy

BATPCAH
Start date: January 2007
Phase: Phase 4
Study type: Interventional

Intravenous patient-controlled analgesia (PCA) is a popular technique for postoperative pain management. Although several drugs are recognized as effective therapeutic options, optimal selection of drugs in hysterectomy patients underwent different anesthesia treatments remains unknown explicitly. The investigators hypothesized that butorphanol and tramadol can produce different analgesic effects with intravenous PCA after abdominal hysterectomy.

NCT ID: NCT00508976 Completed - Pain, Postoperative Clinical Trials

Clinical Proposal for the Comparison of Intraperitoneal Anesthetic to Injected Local Anesthetic

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

The purpose of this study is to determine if pre-incisional lidocaine injection, instilled liquid bupivacaine, intra-abdominal aerosolized bupivacaine, or post-operative bupivacaine injection is superior in post-operative pain control in laparoscopic bariatric surgical patients.