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Pain, Postoperative clinical trials

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NCT ID: NCT02751346 Completed - Pain Clinical Trials

Persistent Pain After Cystectomy for Bladder Cancer

Start date: January 2016
Phase:
Study type: Observational

This single-center, cross-sectional survey and sensory examination is conducted to determine the prevalence, sensory characteristics and risk factors of PPSP in patients who underwent cystectomy at Washington University/Barnes-Jewish Hospital between 2009 and 2015. Based on data from other lower abdominal surgeries, the investigators hypothesize that 10-15% of patients undergoing cystectomy will develop PPSP.

NCT ID: NCT02750917 Completed - Postoperative Pain Clinical Trials

Lornoxicam Versus Etoricoxib in Postoperative Pain After Total Knee Arthroplasty

Start date: September 2014
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess efficacy and safety of lornoxicam compared with that of etoricoxib after total knee replacement.

NCT ID: NCT02749162 Completed - Postoperative Pain Clinical Trials

Perineural Dexamethasone in Femural Nerve Block After Ligament Reconstruction

Start date: November 2015
Phase: Phase 3
Study type: Interventional

The effect of perineural dexamethasone administered as an adjuvant in prolonging the duration of analgesia continues to be under debate. The investigators performed a prospective randomized study to evaluate the effect of perineural dexamethasone in different concentrations in postoperative analgesia in femoral nerve block for anterior cruciate ligament reconstruction.

NCT ID: NCT02747875 Terminated - Clinical trials for Opioid Use, Unspecified

Methadone vs. Fentanyl Administration on Postoperative Pain Control in Pediatric Patients Undergoing Cardiac Surgery

CV_RCT_M_F
Start date: September 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if methadone improves postoperative pain control in pediatric patient's undergoing cardiac surgery.

NCT ID: NCT02747628 Completed - Clinical trials for Postoperative Pain Relief

Transdermal Nicotine and Melatonin Patches for Postoperative Pain Relief

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

Sixty female non-smoker patients, aged 18-50 years and ASA I and II undergoing elective laparoscopic cholecystectomy under general anesthesia were included in this randomized controlled double-blind study. Patients were randomly divided into 3 groups 20 each, C group patients received transdermal placebo patch, TDN group (15 mg/16 h) and TDM group (7 mg/8h). Assessment of postoperative pain, sedation, hemodynamic variables such as HR and MAP, postoperative monitoring of arterial SpO2 and side effects (e.g. nausea, vomiting, pruritis, respiratory depression and hemodynamic instability) were done 30 minutes, 1, 2, 6 and 12 hours postoperatively. Postoperative Patient's and Surgeons' satisfaction, Intraoperative bleeding and plasma cortisol (µg / dl) 2 hours postoperatively were also assessed.

NCT ID: NCT02746263 Terminated - Clinical trials for Acute Pain, Postoperative

Multicenter Study to Compare Intravenous and Oral Acetaminophen for the Treatment of Acute Moderate to Severe Pain

Start date: April 27, 2016
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare intravenous (IV) and oral acetaminophen for the treatment of acute moderate to severe pain in combination with standard patient-controlled analgesia (PCA) in adult subjects following total knee replacement.

NCT ID: NCT02744352 Terminated - Clinical trials for Distal Radius Fracture

Single Shot vs Catheter Infraclavicular Brachial Plexus Block After Distal Radius Fracture Repair

Start date: October 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to compare infraclavicular brachial plexus shot single shot block to continuous catheter nerve block done in adult patients who have under gone surgery to repair distal radius fractures. Visual analogue scores, opioid consumption, quality of recovery and quality of sleep up to 72 hours post operatively will be used for comparison.

NCT ID: NCT02741492 Completed - Post-Operative Pain Clinical Trials

Transversus Abdominus Plane Catheters for Open Inguinal Hernia Repair

Start date: April 2016
Phase: N/A
Study type: Interventional

This study is designed to evaluate pain control of continuous transversus abdominis plane (TAP) blocks placed for open inguinal hernia repair. The investigators hypothesize that there will be improved pain control when compared with sham blocks.

NCT ID: NCT02741219 Completed - Postoperative Pain Clinical Trials

A Multicenter Study: Dexmedetomidine Combined With Sufentanil for Patient Controlled Intravenous Analgesia After Caesarean Section

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

The purpose of this multicenter study is to evaluate the effectiveness and safety of dexmedetomidine combined with sufentanil for patient-controlled analgesia after caesarean section

NCT ID: NCT02738710 Completed - Pain, Postoperative Clinical Trials

Comparison of Post-operative Pain at Umbilical Wound After Laparoscopic Cholecystectomy With Transumbilical Versus Infraumbilical Incision

Start date: September 2016
Phase: N/A
Study type: Interventional

This study compare outcomes (i.e. pain, wound infection, and patient satisfaction) between infra-umbilical vs. trans-umbilical incision after Laparoscopic cholecystectomy