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Postoperative Pain clinical trials

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NCT ID: NCT02090790 Recruiting - Postoperative Pain Clinical Trials

Comparison of Analgesic Consumption Between Perioperative ıv Dexamethasone and Added to Femoral Block

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

the aim of this study was to investigate compare the effect of peroperative intravenous single dose dexamethasone and the addition of dexamethasone to femoral nerve block on postoperative analgesic consumption and patient comfort in unilateral total knee arthroplasty patients

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: NCT01726192 Recruiting - Postoperative Pain Clinical Trials

Comparison of Two Techniques for Placement of Perineural Femoral Catheters.

HLOCSTIM2
Start date: August 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the efficacy of the hydrolocalization technique for placement of femoral perineural catheters in comparison with stimulating catheters. A non inferiority trial.

NCT ID: NCT01623635 Recruiting - Postoperative Pain Clinical Trials

Intraperitoneal Atomization of Ropivacaine During Gynecologic Laparoscopic Surgery

Start date: February 2012
Phase: Phase 3
Study type: Interventional

Pain following laparoscopic surgery continues to be a clinically important problem with 80% or more patients requiring opioid analgesia post-operatively to control their pain. By reducing this surgical complication patients can experience less discomfort and be discharged from the recovery room more rapidly leading to reduced resource utilization and expense. HYPOTHESIS: Post-operative pain after laparoscopic procedures could be treated by topical anesthetics sprayed directly into the abdomen (inside the abdominal cavity, on the nerve endings of the visceral peritoneal lining and diaphragm surface) via the surgical incision METHODS: Randomized controlled trial on use of topical anesthetic (namely 0.25% ropivacaine) delivered directly onto the target sites both at the beginning and the end of surgery in patients undergoing laparoscopic gynecologic procedure for uterine or adnexal benign pathology. The drug will be delivered using a CE approved delivery system that will direct a fine mist of drug directly to the areas of the peritoneal cavity that are theoretically the cause of post-op pain (diaphragms, peritoneal abdominal surface, surgical dissection site). GOAL: to assess the efficacy of intraperitoneal topical anesthesia in reducing postoperative pain, opioid requirements in patients undergoing laparoscopic gynecologic procedure for uterine or adnexal benign pathology

NCT ID: NCT01608373 Recruiting - Postoperative Pain Clinical Trials

The Effect of Intravenous Lidocaine and Intraperitoneal Lidocaine Irrigation on Pain After Laparoscopic Cholecystectomy

Start date: July 2011
Phase: Phase 4
Study type: Interventional

This prospective randomized study aims to comparison the effectiveness of intravenous lidocaine injection and intraperitoneam lidocaine irrigation on the relief of pain in patients undergoing laparoscopic cholecystectomy. A total of 83 patients will be randomized into one of three groups (group C or group I or group P) based on Excel number generation. Patients in group C will receive normal saline intravenous injection, and patients in group I will receive an intravenous bolus injection of 1.5 mg/kg lidocaine followed by a continuous lidocaine infusion of 2 mg/kg/hr. Patients in group P will receive intraperitoneal lidocaine irrigation with 3.5 mg/kg lidocaine and normal saline 100cc. Visual analogue scale pain scores, fentanyl consumption and the frequency at which patients pushed the button (FPB) of a patient-controlled analgesia system will be recorded at 2, 4, 8, 12, 24, 48 hours postoperatively.

NCT ID: NCT01608360 Recruiting - Postoperative Pain Clinical Trials

The Effect of Intravenous Lidocaine on Pain After Thyroidectomy

Start date: July 2011
Phase: Phase 4
Study type: Interventional

This prospective randomized study aims to evaluate the effectiveness of intravenous lidocaine injection on the relief of pain in patients undergoing thyroidectomy. A total 56 patients will be randomized into one of two groups(group C or group I) based on Excel number generation. Patients in group C will receive normal saline intravenous injection, and patients in group I will receive an intravenous bolus injection of 1.5mg/kg lidocaine followed by a continuous lidocaine infusion of 2mg/kg/hr. Visual analogue scale pain scores, fentanyl consumption, the frequency at which patients pushed the button(FPB) of a patient-controlled analgesia system, and presence or absence of nausea and vomiting will be recorded at 2,4,8,12,24,48 hours postoperatively.

NCT ID: NCT01595165 Recruiting - Postoperative Pain Clinical Trials

Transversus Abdominis Plane Block and Postoperative Pain After Laparoscopic Cholecystectomy

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

Transversus abdominis plane (TAP) block has gained popularity for the control of postoperative pain in various surgeries. Three studies showed inconsistent result on pain control after TAP block in laparoscopic cholecystectomy. The TAP technique used in these studies was classic ultrasound guided TAP block. Besides periumbilical incision, sub-xiphoid incision is usually made during laparoscopic cholecystectomy. As typical posterior TAP rarely extend above T8, the investigators undergo subcostal TAP block for this type of surgery. The investigators are going to investigate the effect of subcostal TAP on early postoperative pain after laparoscopic cholecystectomy.

NCT ID: NCT01542697 Recruiting - Postoperative Pain Clinical Trials

Effect of Intraperitoneal Nebulisation of Magnesium Sulphate for Analgesia Following Laparoscopic Cholecystectomy

Start date: June 2011
Phase: Phase 4
Study type: Interventional

intraperitoneal nebulisation with magnesuim sulphate will reduce post operative pain and analgesic consumption in postoperative period following laparoscopic cholecystectomy.

NCT ID: NCT01530815 Recruiting - Postoperative Pain Clinical Trials

Bupivicaine to Reduce Postoperative Pain in Laparoscopic Ventral Hernia Repair

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

The investigators are testing to see if infusion of bupivicaine between the mesh and abdominal wall can reduce postoperative pain and decrease use of narcotics in the postoperative setting.

NCT ID: NCT01485939 Recruiting - Postoperative, Pain Clinical Trials

Lidocaine Patch for Postoperative Analgesia After Laparoscopic Cholecystectomy

Start date: November 2011
Phase: Phase 4
Study type: Interventional

The investigators hypothesized that application of a 5% lidocaine patch would be associated with reduced pain scores after operation compared with placebo patch in patients undergoing laparoscopic cholecystectomy.