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Acute Pain clinical trials

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NCT ID: NCT02957097 Withdrawn - Pain, Postoperative Clinical Trials

Gabapentin as a Pre-emptive Analgesic in Oral and Maxillofacial Surgical Procedures

Start date: September 2019
Phase: Phase 4
Study type: Interventional

The purpose of this study is to assess the effectiveness of pre-operative administration of gabapentin 900 mg in management of acute post-operative pain in patients undergoing oral and maxillofacial surgical procedures.

NCT ID: NCT02935933 Active, not recruiting - Chronic Pain Clinical Trials

Paravertebral Morphine Versus Dexmedetomidine on Acute and Chronic Postmastectomy Pain

Start date: October 2016
Phase: Phase 1/Phase 2
Study type: Interventional

Evaluate the effect of addition of morphine, dexmedetomidine to bupivacaine in PVB could improve the analgesic effect and thus reduce postoperative morphine consumption and development of chronic neuropathic pain, compared to PVB with bupivacaine , in patients undergoing major breast cancer surgery, i.e., modified radical mastectomy (MRM) and breast conservation surgery with axillary lymph node dissection.

NCT ID: NCT02929524 Completed - Acute Pain Clinical Trials

Intranasal Ketamine as a Sedative for Venipuncture

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

Randomized clinical trial, controlled, double-blind, parallel two-arm.

NCT ID: NCT02926573 Completed - Postoperative Pain Clinical Trials

Perioperative Gabapentin Use In Head And Neck Mucosal Surgery Patients

GABA
Start date: June 24, 2016
Phase: Phase 4
Study type: Interventional

Patient satisfaction with healthcare is increasingly being utilized as a metric to reflect provider and hospital quality of care. Furthermore, at the core of a healthcare team and healthcare system is the desire to provide patients with the best possible care in order to achieve the best possible outcomes. Providers have the duty to identify areas of needed improvement within the domains of treatment. An area of need that is ubiquitous within medicine is pain control; in this case acute postoperative pain control is the targeted condition. Studies have already shown that better control of acute postoperative pain leads to shortened hospital stays, reduced hospital costs and patient morbidity, improved patient satisfaction and a reduced likelihood of developing chronic pain. Research within the field of pain management has definitively revealed that a combination of different medication regimens can control acute postoperative pain better than narcotics alone. In particular, the medication gabapentin has been shown to improve acute postop pain in many kinds of surgical settings, and it is a safe medication with arguably fewer side effects than narcotics. The investigators know that certain groups of post surgical otolaryngology patients can be at risk for high levels of postoperative pain. Given all of this information, physicians have a responsibility to utilize medications such as gabapentin to do a better job of controlling patient's pain. This investigation is a quality improvement project designed to elucidate the benefits of gabapentin in pain management in patients undergoing surgery of the head and neck mucosal surfaces. It will provide much needed data in an understudied population and ultimately will improve the practice of pain management, patient satisfaction and quality of care delivered in the Barnes otolaryngology department.

NCT ID: NCT02920528 Completed - Chronic Pain Clinical Trials

Subdissociative Dose Ketamine for Treatment of Acute Pain in Subjects With Chronic Pain

Start date: May 1, 2017
Phase: Phase 3
Study type: Interventional

This is a prospective, randomized controlled trial which will be conducted to determine whether sub-dissociative dose ketamine (SDDK) can improve pain control in subjects with chronic pain syndrome presenting to the emergency department with exacerbation of their chronic pain. The investigators also aim to determine whether use of SDDK can reduce the amount of subsequent opioid pain medications required for adequate pain relief in this population.

NCT ID: NCT02914678 Completed - Acute Pain Clinical Trials

Is There an Ideal Dose of Intravenous Fentanyl in the Prehospital Setting

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

In a previous study the investigators evaluated the apparent efficacy and safety of intravenous fentanyl administered by ambulance personnel and found that 58.4% (CI 56.4-60.4) out of 2348 prehospital patients treated with fentanyl still experienced moderate to severe pain [numeric rating scale (NRS, 0-10) > 3] at hospital arrival. The number of patients with possible fentanyl-related side effects was low. Therefore, the aim of the present study is to explore the efficacy and safety of a liberalized pain treatment protocol for ambulance personnel (a total of 3 μg/kg per transport) compared with existing restrictive protocol (a total of 2 μg/kg per transport). The investigators hypothesize that: - A higher proportion of patients will experience sufficient pain relief at hospital admission (NRS < 4) using the liberalized protocol and - There will be no differences in the proportion of potential fentanyl related side-effects are observed.

NCT ID: NCT02910167 Completed - Acute Pain Clinical Trials

Observational Prospective Study to Evaluate AEs, Risk Factors and Drug Utilization of BUSCAPINA COMPOSITUM N in Adults From Metropolitan Lima

Start date: October 15, 2016
Phase:
Study type: Observational

What AE occur in routine clinical practice, what is the incidence of AE and Adverse Drug Reaction, how many patients present with AE symptoms related to a potential liver injury. What are the drug utilization patterns in patients, what are the predisposing factors for the occurrence of adverse events and adverse drug reactions.

NCT ID: NCT02862769 Recruiting - Chronic Pain Clinical Trials

Intra-operative Lidocaine Infusion in Preventing CPSP Post VATs

Start date: January 1, 2017
Phase: Phase 4
Study type: Interventional

The aim of this study is to evaluate the impact of intravenous lidocaine on acute and chronic post surgical pain on patients undergoing video assisted thoracoscopic surgery(VATS). The investigators believe that systemic administration of lidocaine during the perioperative period would be effective in preventing chronic pain post VATS. In addition to chronic pain the investigators believe it will reduce acute postoperative pain as well as each patients total opioid requirement.The investigators believe that this will have a significant impact on the care of patients presenting for VATS.

NCT ID: NCT02856750 Completed - Acute Pain Clinical Trials

Efficacy of Gabapentin vs. Placebo for Adjuvant Pain Control Following Acute Rib Fractures

Start date: October 2016
Phase: Early Phase 1
Study type: Interventional

A Multi-center, Randomized Controlled Trial of the Efficacy of Gabapentin vs. Placebo for Adjutant Pain Control Following Acute Rib Fractures.

NCT ID: NCT02846610 Terminated - Pain, Postoperative Clinical Trials

Registry for Acute Pain Treatment

Start date: September 2007
Phase:
Study type: Observational [Patient Registry]

The German Network for acute pain management and Regional Anesthesia (NRA) is a multi-center, non-interventional registry and benchmark project, assessing and analysing clinical and patient-reported procedural and outcome data of systemic analgesia and regional anesthesia hosted by the German Society of Anesthesia and Intensive Care Medicine (DGAI) and professional Society German Anesthetists (BDA)