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Pain, Postoperative clinical trials

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NCT ID: NCT01981291 Completed - Postoperative Pain Clinical Trials

Duration of Sciatic Nerve Block After Injection of Local Anesthetic In or Around the Nerve

Start date: October 2012
Phase: Phase 4
Study type: Interventional

This study was designed to assess whether the injection of local anesthetic into the nerve (intraneural), as opposed to around it (perineural), leads to longer anesthesia and analgesia of the leg. Some reports of accidental intraneural injection mention an extremely long duration. When different drugs and doses were evaluated in a clinical trial of intraneural injection, a longer-than-expected duration was reported. The investigators will compare the two types of injection using the same drug, so as to determine if there is an actual difference in duration.

NCT ID: NCT01979354 Recruiting - Postoperative Pain Clinical Trials

0.15 mg Spinal Morphine vs. no Treatment for Morphine Requirement After VATs.

Start date: February 2014
Phase: Phase 4
Study type: Interventional

Postoperative pain after Video-assisted Thoracoscopic Surgery (VAT) is still debating. Therefore the investigators conduct a study comparing 0.15 mg spinal morphine and control group in term of analgesia.

NCT ID: NCT01977937 Completed - Pain, Postoperative Clinical Trials

Pain Control in Pediatric Posterior Spine Fusion Patients: The Effect of Gabapentin

Start date: November 2013
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the patient experience when using gabapentin with other pain control medications after posterior spinal fusion surgery for scoliosis in adolescents. These results will be compared to patients who underwent the same procedure during the study period and received the same standardized pain control regimen excluding gabapentin. Effects on pain level, opioid use, and satisfaction will be measured. Opioid side effects including nausea, sedation and urinary retention (inability to empty one's bladder) will also be recorded.The null hypotheses are as follows: 1. There is no significant difference in pain control when adding gabapentin to a multimodal pain management protocol in pediatric post-operative posterior spinal fusion patients. 2. There is no significant difference in the amount of opioid medication required for pain control in pediatric post-operative posterior spinal fusion patients.

NCT ID: NCT01976403 Completed - Pain Clinical Trials

Intervention Study to Enhance Patients' Pain Management After Cardiac Surgery

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

The main objective of this randomized controlled trial is to evaluate the effect of an intervention formed as a pain booklet provided to patients at discharge from hospital following cardiac surgery. The primary objectives are to: 1. Develop and implement a pain booklet to improve pain management after cardiac surgery 2. Evaluate the effect of the pain booklet compared to a group of patients given usual care

NCT ID: NCT01974843 Completed - Pain, Postoperative Clinical Trials

Caudal Block With Tramadol and Levobupivacaine or Bupivacaine

Start date: January 2011
Phase: N/A
Study type: Observational [Patient Registry]

Caudal block is the regional anesthetic technique that is used most frequently in pediatric surgery. Opioid drugs have been added to local anesthetic solutions to prolong duration of analgesia but ideal combination were not found that has minimal adverse effect. The aim of this study was to compare the postoperative analgesic efficacy of equal concentrations of bupivacaine plus tramadol or levobupivacaine plus tramadol in pediatric patients undergoing minor urological surgery.

NCT ID: NCT01969006 Withdrawn - Clinical trials for Post Operative Pain as Estimated by the Sue of the VAS Score

Ilioinguinal Block in Laparoscopic Inguinal Hernia Repair

Start date: January 2014
Phase: Phase 2
Study type: Interventional

This study is undertaken to clarify whether intraoperative blockage with 40 ml of ½ % Marcaine© of the nerves in the ilio-inguinal canal may decrease postoperative pain after laparoscopic inguinal hernia repair. Patients will be randomised to injection of Marcaine© og a needle prick per-operatively. Pain will be estimated using the VAS score in: 1. the wound 2 the abdomen 3 the shoulder Scoring will be performed: 1. pre-operatively 2. 1 hour postoperatively 3. at discharge from the hospital d day 1,2 and 3 post OP e. 1 year post OP

NCT ID: NCT01966250 Completed - Low Back Pain Clinical Trials

Electroacupuncture as a Complement to Usual Care for Patients With Non-acute Pain After Back Surgery

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

The purpose of this study is to find out the effectiveness of integrative medicine model for pain relief and improvement of function and quality of life on the patients with pain after back surgery.

NCT ID: NCT01966172 Completed - Postoperative Pain Clinical Trials

Multimodal Analgesic Treatment Versus Traditional Morphine Analgesia After Cardiac Surgery

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

To test if multimodal analgesia with different analgesic medication offer better pain relief, lesser side effects and is safe compared to conventionel opiod analgesia after cardiac surgery.

NCT ID: NCT01964781 Completed - Pain, Postoperative Clinical Trials

The Effect of Topical Administration of Common Drugs on Postoperative Bleeding and Pain

Start date: August 2013
Phase: Phase 4
Study type: Interventional

After surgical procedures, interventions to reduce postoperative pain and bleeding are of great importance. In this study, the effect will be investigated of smearing common drugs, which are designed for injection, directly onto the raw wound surface (topical application) created during surgery. Topical application allows a small amount of drug to reach a large wound area, higher drug concentration in the exposed wound surface but very low concentration in the body, and no risk of injury from needles. Although beneficial effects of such an easy and low-cost intervention would be expected, the investigators have found no previous reports on blinded and controlled studies.

NCT ID: NCT01960049 Completed - Postoperative Pain Clinical Trials

Novel Technique of Analgesia Following Open Liver Resection

Start date: October 2013
Phase: Phase 4
Study type: Interventional

Abdominal wall incisions used for liver surgeries are associated with significant postoperative pain and disability. Epidural analgesia is often contraindicated in these patients due to common bleeding problems. Furthermore, drugs such as acetaminophen and opioids are often inadequate and can lead to detrimental side-effects. Abdominal wall (AW) catheters can be placed during surgical closure along the incision line and can be used to administer local anesthetics for postoperative pain. The study is a multi-centre, double-blind, randomized controlled trial involving 120 patients undergoing elective liver surgery. Patients will be randomly assigned to AW catheter group treated with drug or control treated with saline. Treatment group will receive AW catheters with ropivacaine plus standard patient controlled analgesia (PCA). Control group will obtain AW with normal saline and no local anesthetics and PCA. Patients are followed for 6 months post-operatively for pain scores, side-effects, chronic pain and complications.