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Postoperative Pain clinical trials

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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: 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: 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: NCT02475031 Completed - Postoperative Pain Clinical Trials

Single-shot TAP Block vs Continuous TAP Block

TAP
Start date: July 2012
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether continuous transversus abdominis plane (TAP) block is superior to single shot TAP for postoperative pain after laparoscopic donor nephrectomy

NCT ID: NCT02468934 Completed - Pain Clinical Trials

Electrical Stimulation for the Treatment of Pain Following Total Knee Arthroplasty (TKA) Using the SPRINT System

Start date: October 22, 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if electrical stimulation (small levels of electricity) can safely and effectively reduce pain following total knee replacement (or total knee arthroplasty (TKA)). This study involves a device called the SPRINT System. The SPRINT System delivers mild electrical stimulation to nerves in the leg that received the knee replacement. The SPRINT System includes a small wire (called a "lead") that is placed through the skin in the upper leg. It also includes a device worn on the body that delivers stimulation (called the SPRINT Stimulator).

NCT ID: NCT02466542 Completed - Postoperative Pain Clinical Trials

Analgesic Effect of Intraoperative Esmolol in Mastectomies

Esmobreast
Start date: June 2015
Phase: Phase 4
Study type: Interventional

This study aims to compare the quality of perioperative analgesia of esmolol in patients undergoing mastectomy.

NCT ID: NCT02462174 Completed - Postoperative Pain Clinical Trials

Topical Ketamine Versus Caudal Ketamine for Postoperative Analgesia in Children Undergoing Inguinal Herniotomy

TKversusCK
Start date: May 2015
Phase: Phase 2/Phase 3
Study type: Interventional

To find alternatives to caudal analgesia that could be more safe and effective and to demonstrate the analgesic efficacy of topical ketamine.

NCT ID: NCT02456909 Completed - Postoperative Pain Clinical Trials

Patient Controlled Analgesia Pump Cues on Patient Satisfaction

PCA Cues
Start date: April 2015
Phase: N/A
Study type: Interventional

To examine whether providing patients with a cue to the availability of pain medication affects patient satisfaction, patient anxiety, PCA efficacy, and safety.