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Postoperative Pain clinical trials

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NCT ID: NCT02691403 Not yet recruiting - Postoperative Pain Clinical Trials

Quadratus Lumborum Block for Postoperative Analgesia After Colostomy Closure

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

Patients undergoing abdominal procedures often require multimodal postoperative pain controls. Truncal blocks such as quadratus lumborum (QL) block may be used adjunctively as a part of it. The investigators hypothesized that the ultrasound-guided QL block with transmuscular approach can provide adequate pain relief for colostomy closure as part of a multimodal pain control.

NCT ID: NCT02460627 Not yet recruiting - Postoperative Pain Clinical Trials

Topical Lidocaine After Arthroscopy on Knee

Start date: May 2015
Phase: Phase 1
Study type: Interventional

More than half of the patients suffer from intensive pain 1-2 days after arthroscopy in the knee. Walking function and physical activities are affected by this intensive pain although local anaesthetic is given in the joint and soft tissue. The patients are often discharged on the same day as the arthroscopy takes place depending on their ability to walk with or without assistive technology. It is a well-known fact that the patient is given a dose of morphine, analgesics or an ice pack on a painful knee to reduce pain intensity. The aim of the project is to study whether pain intensity and analgesics can be additionally reduced by giving local anaesthetic by means of an adhesive tape placed on the skin instead of giving morphine, analgesics or ice pack on a painful knee. The researchers plan to include a cohort of 180 patients: 60 patients having a meniscus sutured, 60 patients having meniscus tissue removed surgically, 60 patients having mucous fold removed surgically. This study is planned to be a pilot study in order to complete a future large medical science study.

NCT ID: NCT02255955 Not yet recruiting - Postoperative Pain Clinical Trials

Postoperative Analgesia in Laminectomy

(PAL)
Start date: October 2014
Phase: Phase 4
Study type: Interventional

Compare the analgesic effects of naproxen sodium codeine, paracetamol codeine and placebo on postoperative pain and tramadol (Contramal) consumption during the first 24 hour after a lumbar disk surgery.

NCT ID: NCT02216682 Not yet recruiting - Postoperative Pain Clinical Trials

Assessing the Efficacy of Intravenous Acetaminophen Versus the Oral Formulation for Perioperative Pain Treatment

Start date: August 2014
Phase: N/A
Study type: Observational

To compare oral (PO) to intravenous (IV) acetaminophen with postoperative pain scores, and consumptions of opiates, among orthopedic surgery patients undergoing total knee replacement with spinal anesthesia. Our hypothesis is that IV acetaminophen patients will have improved analgesia, less opioid consumption, a lower percentage of patients rescuing, or a longer time to first rescue with IV acetaminophen. The investigators will compare the efficacies of oral and intravenous acetaminophen for postoperative pain control, and utilization of opiates as rescue agents.

NCT ID: NCT01909765 Not yet recruiting - Postoperative Pain Clinical Trials

Two Different Surgical Techniques on Postoperative Circumcision Pain

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

To compare the effect of two different surgical techniques, the dorsal slit and double incision technique, on postoperative pain.

NCT ID: NCT01359059 Not yet recruiting - Postoperative Pain Clinical Trials

Pre- Versus Post-incisional Pregabalin for Postoperative Pain Attenuation and Analgesics Spare in Orthopedic Oncologic Patients

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

Hypothesis No studies considered the comparison of preemptive vs. post-surgery Pregabalin (PGL) only administration. The investigators believe that the administration of PGL preemptively would diminish pain sensation and therefore the need for opioids administration in orthopedic-oncologic patients more effectively than if administered starting postoperatively.

NCT ID: NCT01291979 Not yet recruiting - Postoperative Pain Clinical Trials

The Effect of Intravenous Lidocaine on Pain After Tonsillectomy

Start date: February 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 tonsillectomy. A total of 62 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 received 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. 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 4, 12, 24, 48 hours postoperatively.

NCT ID: NCT01069055 Not yet recruiting - Postoperative Pain Clinical Trials

Comparison of Lornoxicam and Paracetamol for Pre-emptive Intravenous Analgesia for Elective Inguinal Hernia Repair

Start date: February 2010
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether lornoxicam or paracetamol is more effective in providing pre-emptive analgesia for adult patients undergoing elective unilateral inguinal hernia repair under general anesthesia.

NCT ID: NCT01024348 Not yet recruiting - Postoperative Pain Clinical Trials

Safety and Effectiveness of Tramadex-OD After Knee Arthroscopy

Start date: December 2009
Phase: N/A
Study type: Interventional

Extended-release tramadol is indicated for the management of moderate to severe pain in adults who require around-the-clock treatment. It provides an extended duration of action, more constant plasma concentrations, a reduced dosing frequency, and the potential for improved compliance and therapeutic outcomes. The present study was designed to evaluate the safety and effectiveness of this medication in the treatment of early postoperative pain after knee arthroscopy.

NCT ID: NCT00822133 Not yet recruiting - Postoperative Pain Clinical Trials

Percutaneous Ketamine Versus Lidocaine or Placebo, for Post-Surgery Analgesia, in Patients Undergoing Laparoscopic Partial Lung Resection

Start date: February 2009
Phase: Phase 4
Study type: Interventional

Since VAT bears with it severe postopearive pain, and since ketamine has been shown to be an optimal analgesics adjuvant for postoperative pain, we wish to assess to effects of ketamie vs. lidocaine if put on the skin in the sites where scopes are interset into the chest for thoracoscopy.