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Pain, Postoperative clinical trials

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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: NCT02718976 Completed - Pain, Postoperative Clinical Trials

Shamrock - Ultrasound/MR Image Fusion Guided Lumbar Plexus Block

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

The main objective is to complete a double-blinded randomized controlled crossover trial of lumbar plexus block with the Shamrock technique guided by ultrasound (US)/magnetic resonance imaging (MRI) image fusion vs. the Shamrock technique guided by ultrasound in healthy volunteers. The investigators will assess block procedure-related parameters, anatomical spread of local anesthetic, and motor and sensory effects.

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

NCT ID: NCT02711501 Completed - Post-operative Pain Clinical Trials

Comparison of Post-operative Complications of Bone Augmentation at Anterior of Maxilla After Periosteal Releasing Incision With Two Techniques Diode Laser and Scalpel

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

The aim of this study was to investigate if using lasers instead of scalpel for flap advancement in bone augmentation procedures would reduce post-operative swelling and pain.

NCT ID: NCT02703259 Completed - Pain, Postoperative Clinical Trials

Single Dose Preoperative Gabapentin Use in Minimally Invasive Hysterectomy for Acute Pain Management

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

The purpose of the investigators' study is to assess the efficacy of a single dose of preoperative gabapentin within an enhanced recovery after surgery protocol in acute postoperative pain reduction for women undergoing a minimally invasive hysterectomy. Participants who consent to participate will be randomized to either a control group without gabapentin or to a study arm and receive gabapentin 600 mg prior to their planned surgery. The investigators will collect data on postoperative narcotic use, subjective pain as rated by a numeric pain scale, in addition to any adverse effects of single dose gabapentin use.

NCT ID: NCT02701114 Completed - Post-Operative Pain Clinical Trials

Proximal Versus Distal Adductor Canal Blocks for Total Knee Arthroplasty

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

This study is designed to evaluate pain control of continuous adductor canal blocks placed proximally versus distally within the canal. The investigators hypothesize that there will be similar pain control between both groups.

NCT ID: NCT02698995 Completed - Postoperative Pain Clinical Trials

Perineural Low-dose Dexamethasone Added to Infraclavicular Block Anesthesia

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

Dexamethasone has an evidence-based indication in postoperative emesis prophylaxy and as a antiinflammatory steroid. Although the perineural administration is off-label, several studies recognised its analgetic action as an adjuvant for peripheral nerves blockade, permitting to reduce the concentration of the local anesthetics and extending the sensory and motor block.Questions remain concerning the mechanism of action, optimal dose, the lack/degree of toxicity and the comparison with intravenous administration.The aim of this prospective randomized controlled study is to investigate the efficacy of analgesia with 4 mg or 2 mg Dexamethasone added to a combination of ropivacaine 0,5% and lidocaine 1% in vertical infraclavicular blockade (VIB) anesthesia for upper limb surgery.

NCT ID: NCT02697955 Completed - Arthritis Clinical Trials

The Effect of Subsartorial Saphenous Block on Postoperative Pain Following Major Ankle and Hind Foot Surgery

Start date: June 21, 2016
Phase: Phase 4
Study type: Interventional

The study investigates the effect of a ultrasound-guided subsartorial saphenous block on postoperative pain following major ankle and hind foot surgery.