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Post-operative Pain clinical trials

View clinical trials related to Post-operative Pain.

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NCT ID: NCT02435459 Recruiting - Dental Caries Clinical Trials

The Effect of Different Lining Strategies on Amalgam Restorations

Start date: April 2012
Phase: N/A
Study type: Interventional

The aim of this research is to compare the clinical outcome of amalgam restorations placed in conjunction with three different lining protocols, each of which represents a different therapeutic concept.

NCT ID: NCT02180087 Recruiting - Cardiac Surgery Clinical Trials

Reduce Nonsteroidal Antiinflammatory Drugs Doses for Analgesia After Sternotomy

LoDoNSAID
Start date: February 2014
Phase: Phase 2
Study type: Interventional

Currently, the management of pain after cardiac surgery is based on the concept of multimodal analgesia: Combined use of non-opioid analgesics associated with morphine intravenous analgesia by a system controlled by the patient (patient-controlled analgesia-PCA). The combination of paracetamol and morphine PCA is very effective on pain at rest, but is limited on pain mobilization and causes the problem of side effects associated with opioid (overdose, sedation, respiratory depression, gastrointestinal intolerance, urinary retention ...) which are contributing factors to increase the length of stay in Intensive Care Unit, an additional cost of care and an increase postoperative morbidity and mortality. Methods that have proved their effectiveness on pain and mobilization used in postoperative cardiac surgery are: anti-inflammatory drugs (NSAIDs) and / or loco-regional analgesia techniques. NSAIDs enhance analgesia produced by PCA Morphine and allow a reduction in morphine consumption, improved postoperative pain, decreased sedation and decreased postoperative morbidity and mortality. Adverse effects of NSAIDs are commensurate with their time and exposure dose. Consequently, NSAIDs, in the absence of against-indications, should always be prescribed and used at the lowest effective dose and for the shortest possible time. Some studies have suggested that lower doses of NSAIDs didn't appear to affect their effectiveness. At present, the investigators have no studies that address the hypothesis from which minimum dose of ketoprofen analgesic effect is obtained. The investigators hypothesis is that lower dose ketoprofen may have efficacy on pain in the postoperative mobilization of cardiac surgery. The investigators want to find, in their study, this "optimal" ketoprofen dose which would be the minimum dose for clinical efficacy demonstrated dose. This optimal dose could reduce the number of adverse effects of NSAIDs, but their study will probably not have enough power to prove it. NSAID use at these low doses, in postoperative cardiac surgery, could be extended to patient populations most at risk or for a duration longer than 48 hours.

NCT ID: NCT02083835 Recruiting - Post-operative Pain Clinical Trials

PAIN OUT: Improvement in Postoperative PAIN OUTcome

PAIN-OUT
Start date: January 2009
Phase:
Study type: Observational [Patient Registry]

PAIN OUT is a multi-national, non-interventional registry and benchmark project, assessing and analysing clinical and patient-reported outcome data of postoperative pain.

NCT ID: NCT01927211 Recruiting - Clinical trials for Surgical Site Infection

Prospective Study on Cesarean Wound Outcomes

Start date: July 2013
Phase: N/A
Study type: Interventional

The study will investigate whether the placement of silver plated dressings beginning in the OR will improve wound healing in patients undergoing cesarean delivery compared to traditional Telfa pads. This study will also explore the presumed improvement in scar integrity when silver plated dressings are used compared to Telfa pads. The study will examine post-operative pain by review of anesthesia and analgesic use during hospitalization and scar-related pain scores at the post-operative visits. The study will compare the percentage of patients who develop a surgical site infection after application of silver plated dressings versus standard Telfa dressings. Investigators will also assess the cosmetic appearance of the cesarean section scar at the patient's one week and 6 wekk post-operative visits.

NCT ID: NCT01452633 Recruiting - Post Operative Pain Clinical Trials

Study to Compare Reduction in Pain After Surgery With and Without Local Anesthesia During Laparoscopy

Start date: November 2011
Phase: N/A
Study type: Interventional

This study will help to answer the question, "Does injecting local anesthetic before laparoscopic instrument ports are placed decrease pain after surgery?" Patients participating will be randomly assigned to receive local anesthetic or saline injection at the site of a laparoscopic instrument port as part of their planned surgery. After surgery at 4 and 24 hours the patient will be asked to rate their pain on a simple chart.

NCT ID: NCT00695240 Recruiting - Clinical trials for Pelvic Organ Prolapse

Post-Operative Pain Control Using Direct Continuous Bupivacaine Infusion After Pelvic Organ Prolapse Repair

Start date: April 2007
Phase: Phase 2/Phase 3
Study type: Interventional

This prospective randomized controlled study will determine the efficacy of continuous local anesthesia at decreasing pain scores compared to patient controlled analgesia for pelvic organ prolapse procedures including posterior colporrhaphy and sacrospinous ligament fixation.