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Postoperative Pain clinical trials

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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: NCT02731950 Completed - Pain Clinical Trials

Presternal Bupivacaine Plus Magnesium Sulfate Infusion After Cardiac Surgery

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

Effective pain relief after cardiac surgery has assumed importance with the introduction of fast track discharge protocols that requires early weaning from mechanical ventilation. Inadequate pain control reduces the capacity to cough, mobility, increases the frequency of atelectasis, and prolongs recovery. Infiltration of local anesthetics near the surgical wound has shown to improve early postoperative pain in various surgical procedures. Magnesium is the fourth most plentiful cation in our body. It has antinociceptive effects in animal and human models of pain.

NCT ID: NCT02729935 Completed - Postoperative Pain Clinical Trials

Parecoxib for Treatment of Catheter Related Bladder Discomfort

Start date: March 2016
Phase: Phase 4
Study type: Interventional

Catheter-related bladder discomfort (CRBD) is defined as an urge to void or discomfort in the supra-pubic region; reported postoperatively in patients who have had urinary catheterization intra-operatively. In the present study, the investigators evaluated Parecoxib (P) for preventing CRBD in patients undergoing catheterization after transurethral resection of bladder tumor (TURBT).

NCT ID: NCT02726828 Completed - Postoperative Pain Clinical Trials

intrathecaم Ketamine, Morphine and Both for Lower Abdominal Cancer Surgery Pain

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

this study investigates the analgesic efficacy and other possible effects of ketamine, morphine, and both together when administered intrathecally for control of postoperative pain following lower abdominal cancer surgeries.

NCT ID: NCT02726126 Completed - Postoperative Pain Clinical Trials

Transdermal Fentanyl and Melatonin Patches for Postoperative Pain Relief

Start date: March 2013
Phase: N/A
Study type: Observational

Seventy five patients, aged 18-50 years, ASA I and II undergoing elective single level lumber laminectomy under general anesthesia were included in this randomized controlled double-blind study. Patients were randomly divided into 3 groups 25 each, C group patients received transdermal placebo patch, TDF group (50μg/h) and TDM group (7 mg). 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) postoperatively were also assessed.

NCT ID: NCT02723487 Completed - Postoperative Pain Clinical Trials

Ultrasound Guided Transversus Abdominis Plane Block in Pediatric Surgery

Start date: April 2016
Phase: Phase 2
Study type: Interventional

The primary objective of this study is to assess differences in postoperative pain experienced by pediatric patients having transversus abdominis plane block block with bupivacaine (0.125% and 0.25%) compared with control group will receive conventional iv analgesia after Laparoscopic surgery.

NCT ID: NCT02720406 Completed - Postoperative Pain Clinical Trials

Topical Ketamine Analgesia in Children Undergoing Tonsillectomy: a Clinical and Serum Level Assays Study.

Start date: April 2016
Phase: Phase 2/Phase 3
Study type: Interventional

The aim of this study is to evaluate the analgesia efficacy of local ketamine given by two different doses in pediatric patients undergoing tonsillectomy operations

NCT ID: NCT02716129 Completed - Postoperative Pain Clinical Trials

The Effect of Adding Nalbuphine to Intrathecal Morphine on Analgesic Efficacy and Side Effects After Cesarean Section

Start date: July 2016
Phase: Phase 2
Study type: Interventional

The primary endpoint of this study is to investigate the effect of adding nalbuphine to intrathecal morphine on quality of postoperative analgesia and Morphine related side effects post- cesarean delivery.

NCT ID: NCT02715999 Completed - Postoperative Pain Clinical Trials

Transversus Abdominis Plane Versus Quadratus Lumborum Block for Pediatrics

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

The purpose of this research study is to find the best way to decrease pain in children whom have had low abdominal surgery. Investigators will perform two technique of trunk block; Transversus abdominis plane or Quadratus lumborum block .The method used is often chosen by which one the doctor has more experience using. The Investigator plans to find out if one of the methods is more effective and/or safer than the other method. The results of this study will help learn how to best control pain in children having surgery low abdominal surgery.

NCT ID: NCT02712749 Completed - Anxiety Clinical Trials

Use of Binaural Beat Premedication in Elderly Submitted to Major Orthopedic Surgery

Start date: September 1, 2016
Phase: N/A
Study type: Interventional

The Investigators verify the effectiveness of "Binaural Beats" as premedication instrument in elderly patients submitted to orthopedic surgery to reduce anxiety , post operative pain and morphine consumption