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Postoperative Pain clinical trials

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NCT ID: NCT02501135 Completed - Postoperative Pain Clinical Trials

A Retrospective Investigation of Local Anesthetic Concentrations in Femoral Nerve Block

Start date: June 2015
Phase:
Study type: Observational

The purpose of this study is to retrospectively compare perioperative pain relief and safety in pediatric patients who have received a femoral nerve block with varying concentrations of local anesthetic.

NCT ID: NCT02499341 Completed - Postoperative Pain Clinical Trials

A Comparison Study Between Ketamine Versus Tramadol for Pain Management After Major Upper Abdominal Surgery

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

The purpose of the study is the comparison between ketamine and tramadol, regarding the analgesia quality and efficiency, in patients receiving Patient Controlled Analgesia (PCA) morphine, after major upper abdominal surgeries such as hepatectomies, gastrectomies, Whipple procedures and peripheral pancreatectomies. The goal is to bring out an improved analgesia scheme, which can be applied to the clinical work and refine the analgesia provided for major procedures which require increased postoperative opioids doses. In the study, half of patients will receive continuous intravenous infusion of tramadol and Patient Controlled Analgesia morphine and the other half will receive continuous intravenous infusion of ketamine and Patient Controlled Analgesia morphine postoperatively after major upper abdominal surgery. The successful combination of different drugs targets at the improvement of the analgesia provided, the reduction of complications and the exploitation of the pharmacodynamic properties of each drug.

NCT ID: NCT02495688 Completed - Postoperative Pain Clinical Trials

Regional or General Anesthesia for Distal Radius Fracture Surgery in a Day Surgery Setting

Start date: March 23, 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to compare general and regional anesthesia with regard to postoperative pain in patients who undergo surgery in a day surgery setting due to a displaced distal radius fracture.

NCT ID: NCT02495220 Recruiting - Postoperative Pain Clinical Trials

Efficacy of Dexmedetomidine for Postoperative Analgesia in Infantile Cataract Surgery

Start date: July 2015
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of the present study was to evaluate the efficacy and safety of subtenon block (SB)anesthesia with dexmedetomidine in combination with bupivacaine versus intravenous dexmedetomidine for postoperative analgesia and emesis control in infants undergoing cataract surgery.

NCT ID: NCT02489851 Completed - Postoperative Pain Clinical Trials

Quadratus Lumborum Block vs Tranversus Abdominis Plane Block for Cesarean Section

Start date: June 2015
Phase: N/A
Study type: Interventional

The Quadratus Lumborum block (QLB) was first described by Blanco in 2007. The main advantage of QLB compared to the Transversus Abdominis Plane block (TAP) is the extension of local anesthetic agent beyond the TAP plane to the thoracic paravertebral space. The wider spread of the local anesthetic agents may produce extensive analgesia and prolonged action of the injected local anesthetic solution. Previous studies showed that both TAP block and QLB may reduce morphine requirements in the postoperative period in patients who had cesarean section under spinal anaesthesia. However there are no published reports comparing the 2 techniques. The aim of this randomised controlled, double blinded study is to compare the analgesic efficacy of QLB compared to TAP block in patients who had cesarean section under spinal anesthesia.

NCT ID: NCT02483338 Recruiting - Postoperative Pain Clinical Trials

FASS (Facial Action Summary Score) Scale to Differentiate the Pain of Postoperative Anxiety in Children Under 7 Years

FASS
Start date: July 2011
Phase: N/A
Study type: Interventional

This study aims to evaluate the psychometric validity of FASS (Facial Summary Score Scale) to assess postoperative children pain.

NCT ID: NCT02481570 Completed - Postoperative Pain Clinical Trials

Anesthetic Optimization in Scoliosis Surgery

AIS
Start date: November 2015
Phase: N/A
Study type: Interventional

The standard anesthetic care plan for people having adolescent idiopathic scoliosis surgery will be accompanied by a pharmacokinetic simulation of the administered drugs to suggest opportunities to adjust drug doses to achieve tolerable pain control after surgery, avoid respiratory depression and allow patients to respond quickly either during intraoperative testing or at the conclusion of surgery.

NCT ID: NCT02479165 Completed - Postoperative Pain Clinical Trials

Pain Management After Cardiac Surgery - Opioids or NSAID

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

The aim of this randomized controlled study is to shed light on the analgesic properties and side-effect profile of an opiod-based regimen as opposed to an Ibuprofene based regimen.

NCT ID: NCT02477098 Completed - Postoperative Pain Clinical Trials

Preoperative Versus Postoperative Ultrasound-guided Rectus Sheath Block for Sleep Quality and Cytokines of Patients

Start date: October 2015
Phase: Phase 4
Study type: Interventional

Rectus sheath block (RSB) is used for postoperative pain relief in patients undergoing abdominal surgery with a midline incision. It has proved to be effective in preoperative block, but it has not been previously compared with postoperative block. The aim of the present study is to evaluate postoperative pain, sleep quality and changes in the cytokine levels of patients undergoing gynaecological surgery with RSB performed preoperatively versus postoperatively.

NCT ID: NCT02476370 Recruiting - Anxiety Clinical Trials

Effects of Preoperative Relaxation and Intensified Surgery Education in Patients Undergoing Herniotomy

MBM_Hernio
Start date: June 2015
Phase: N/A
Study type: Interventional

This study aims to test the effects of a Preoperative Relaxation intervention and an Intensified Surgery Patient Education on pre- and postoperative wellbeing and health in Patients Undergoing Herniotomy.