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Pain, Acute clinical trials

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NCT ID: NCT03509857 Completed - Pain, Acute Clinical Trials

Vibration Analgesia in Propofol Infusion During Anesthesia Induction

VAPI
Start date: February 1, 2019
Phase: N/A
Study type: Interventional

In this study, the investigators seek to evaluate the role of vibration in the reduction of discomfort associated with painful stimulus associated with anesthesia induction. Through this study, the investigators hope to develop a comprehensive and cost-effective approach to minimize patient discomfort during anesthesia induction.

NCT ID: NCT03502655 Completed - Pain, Acute Clinical Trials

Discomfort During Intravenous Cannulation in an Emergency Department: Impact of Communication

DOUCIP
Start date: December 13, 2017
Phase: N/A
Study type: Interventional

The main goal of this study is to investigate whether the communication between patients and healthcare providers has an impact on pain and anxiety induced by the insertion of a peripheral venous catheter in an emergency department. Another goal is to determine if the effect is mediated by the content of the message in itself or if it is mediated by non-verbal cues . Therefore, the message will be delivered by either an audio recording in the first phase of the study, and by the healthcare providers themselves in the second phase of the study. A secondary goal is to assess whether there are discrepancies between the patients' pain and anxiety reports and the healthcare providers' evaluation of the patient's pain and anxiety.

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: 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: 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: 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: 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.

NCT ID: NCT03441269 Completed - Pain, Acute Clinical Trials

Adult Oral Ibuprofen Study for ED Pain Patients

Start date: November 1, 2018
Phase: Phase 4
Study type: Interventional

Ibuprofen is one of the most widely used non-steroidal anti-inflammatory drug (NSAID) for management of mild -to moderate pain in the ED (acute musculo-skeletal pain, headache, dental pain). Ibuprofen as a representative of NSAID's as a class follows the analgesic ceiling concept that postulates that there is a dose of a drug beyond which any further dosage increase results in no additional analgesic effect. Despite this fact, Ibuprofen may commonly be used at doses above its analgesic ceiling, although this may not offer an incremental analgesic advantage and potentially adds risk of harm. The analgesic ceiling dose for ibuprofen is only 200-400mg/dose, and about 1200 mg/day. Thus, we hypothesize that administration of Ibuprofen in a dose of 400 mg in the ED is as effective in treating mild-to-moderate acute pain in patients presenting to the ED as 600 mg and 800 mg

NCT ID: NCT03429738 Completed - Pain, Acute Clinical Trials

Single-Dose Bioavailability Study of Two Formulations of Ibuprofen and Pseudoephedrine Hydrochloride Tablets

Start date: April 27, 2014
Phase: Phase 1
Study type: Interventional

Evaluation of the comparative bioavailability between two oral formulations containing ibuprofen 200 mg and pseudoephedrine 30 mg after a single dose in healthy subjects under fasting conditions.

NCT ID: NCT03420911 Completed - Anxiety Clinical Trials

Determination of the Effects of Change in Anxiety Level on Pain Perception in Patients Who Present to Emergency Department

Start date: June 2013
Phase: N/A
Study type: Interventional

The aim of this study is to determine the level of pain and anxiety in patients who present to the emergency department with acute pain, and to investigate the effect of the standard analgesic treatment and an additional anxiolytic treatment on pain and anxiety.