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Acute Pain clinical trials

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NCT ID: NCT03496194 Completed - Anesthesia Clinical Trials

Anaesthesiological Involvement in Postoperative Pain Treatment

Start date: April 13, 2018
Phase:
Study type: Observational

This study aims to investigate the current organization and management of postoperative pain in Denmark, especially for invasive pain treatment modalities (epidural infusions, PCA and regional blocks), in a national survey covering the activities in Danish Hospitals. This study is an electronic questionnaire survey, that aim to describe and map the foundation for future developments within, and improvement of, postoperative pain management.

NCT ID: NCT03495076 Completed - Pain, Acute Clinical Trials

Perceptual Distortions in Acute Neck Pain

Start date: April 20, 2018
Phase: N/A
Study type: Interventional

Research has shown that chronic pain is related to variety of perceptual distortions. Little is known on how acute pain experience influences perception, especially precision of touch. This project is aiming to test the hypothesis of pain as a process of biological value leading to improvement in tactile acuity.

NCT ID: NCT03493191 Completed - Acute Pain Clinical Trials

A Single Dose Study of SHR0410 in Healthy Male Participants

Start date: April 15, 2018
Phase: Phase 1
Study type: Interventional

This is a randomized, double-blind, placebo-controlled, single ascending-dose study to investigate the effect of a single intravenous (IV) dose of SHR0410 at 6 dose levels (0.5 μg/kg, 1 μg/kg, 2 μg/kg, 5 μg/kg, 10 μg/kg and 20 μg/kg) in healthy participants.

NCT ID: NCT03491657 Completed - Pain, Acute Clinical Trials

Virtual Reality Analgesia for Pediatric Burn Survivors

Start date: March 13, 2014
Phase: N/A
Study type: Interventional

Many children with large severe burns report severe pain during burn wound cleaning. The current study explores whether adjunctive immersive Virtual Reality distraction may help reduce the intensity of pain experienced by children during burn wound cleaning by taking the patient's mind off their pain.

NCT ID: NCT03484429 Completed - Chronic Pain Clinical Trials

Postoperative Peripheral Nerve Stimulation for Management of Post-amputation Pain

Start date: December 1, 2017
Phase: N/A
Study type: Interventional

Limb loss is frequently associated with postamputation pain that can be challenging to treat and often involves opioids. Advances in the field of neuromodulation has led to development of an intentionally reversible percutaneous peripheral nerve stimulation (PNS) system that has had promising results when treating chronic postamputation pain. PNS may offer sustained pain relief even after the treatment period has ended. Currently, there is no convincing evidence regarding the role of PNS in the acute postoperative period, which may be a critical time to control pain as those with higher pain appear to be at higher risk for developing persistent post-procedural pain. The investigators of this study aim to evaluate the feasibility and effects of PNS in the acute postoperative period and determine the feasibility of completing a randomized controlled treatment outcome study.

NCT ID: NCT03477851 Completed - Pain, Acute Clinical Trials

Tramadol Simultaneously With Sciatic Nerve Block for Calcaneus Fracture Osteosynthesis

TramIsch
Start date: June 15, 2017
Phase: Phase 4
Study type: Interventional

Comparison of duration of efficient analgesia after painful surgical repair od foot fractures between groups treated with sciatic nerve block alone and sciatic nerve block simultaneously with i.m. tramadol

NCT ID: NCT03468348 Completed - Acute Pain Clinical Trials

Duloxetine for Acute Post-mastectomy Pain

Start date: April 1, 2018
Phase: N/A
Study type: Interventional

The objective of this study is to evaluate the analgesic effect of oral dulexitine tablet (administered 2 h before surgery) as well as the ideal dose for acute postmastectomy pain.

NCT ID: NCT03467685 Completed - Pain, Acute Clinical Trials

Variable Perception of Cutaneous Stimulation

Start date: June 19, 2018
Phase: N/A
Study type: Interventional

Perception of cutaneous sensory stimulation shows a large range of variability across multiple populations. Understanding this variability is critical to medical practice as interpretation of discomfort and pain is critical to diagnosis and treatment. Further, procedural medicine involves inflicting pain on patients in the form of injection of local anesthetic. Our protocol aims to determine how patients differentially interpret the non-noxious stimulation of vibration and the differences in perceiving anesthestic injection after the vibratory stimulus. We will explore how this ranges across all patients treated in a dermatological surgery out-patient setting. The goal is to identify which variables, such as age, gender, medical history, influence how sensation is interpreted.

NCT ID: NCT03456141 Completed - Clinical trials for Pain, Post-operative

Multimodal Analgesic Protocol to Moderate Acute Pain

Start date: March 1, 2018
Phase:
Study type: Observational

With a prospective, observational study assess post-surgery pain levels and patient's use of opioids and other analgesic drugs to moderate pain following third molar surgery.

NCT ID: NCT03450798 Completed - Pain, Acute Clinical Trials

SOFT Block Versus Spinal Anesthesia in Patientsusing Ilizarov External Fixator

Start date: February 10, 2018
Phase: N/A
Study type: Interventional

Peripheral nerve block is an ideal choice for lower limb surgery because of the peripheral site of the surgical procedure and the ability to block pain pathways at multiple levels. On the contrary to other anesthetic techniques, as spinal or general anesthesia, properly performed peripheral nerve blocks bypass adverse events as hemodynamic instability and respiratory complications, properly treat post-operative pain leading to early hospital discharge. Additional advantages of peripheral nerve blocks are that they can be used in patients receiving anti-coagulants or lumbosacral disease in addition to avoidance of airway instrumentation. Recently, there has been a significant interest in regional anesthesia and peripheral nerve blockade. This is facilitated by a significant advance of the research in this field and availability of better equipment facilitating regional anesthesia.The aim of this study was to assess the efficacy and safety of SOFT block (sciatic-obturator-femoral nerve block technique) in comparison with spinal anesthesia in patients undergoing surgery for fixation of open tibial fractures using Ilizarov external fixator.