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Acute Pain clinical trials

View clinical trials related to Acute Pain.

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NCT ID: NCT04283643 Recruiting - Pain, Acute Clinical Trials

Noninvasive Brain Stimulation for Pain Relief

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

Non-invasive brain stimulation techniques, transcranial magnetic stimulation (TMS) and transcranial focused ultrasound (FUS), is be applied to healthy human subjects, acute pain patients, and chronic pain patients to investigate their uses for pain relief.

NCT ID: NCT04281836 Completed - Pain, Acute Clinical Trials

Visual and Auditory Neuromodulation of Pain Perception

Start date: February 11, 2016
Phase: N/A
Study type: Interventional

Medical and dental patients may experience fear commonly attributed to physical pain during the visit. By reducing pain perception, patient comfort and future patient compliance may be improved. Patient health may be improved by increasing compliance and promoting increased visits. This can lead to more frequent and timely preventative actions. The research purpose is to establish quantitative and qualitative data to support current, non-pharmacological methods for reducing pain sensitivity. More specifically, the investigators aim to determine if the use of auditory and visual (3D imaging) stimuli related to the regulation of breathing can decrease or modulate pain. Healthy participants between the ages of 18 and 60 will participate in a one week study, with two in lab appointments on day one and day seven. Participants will be split into two groups, one will undergo breathing awareness using auditory and visual technology (i.e. listen to one's own breathing with headphones and watch 3D image of lungs using virtual headset), and the second group will have breathing awareness without the use of technology (i.e. simply focusing on one's own breathing). At each appointment, the investigators will collect pain threshold data using thermal Quantitative Sensory Testing (tQST) and brain activity data using Functional near-infrared spectroscopy (fNIRS). tQST and fNIRS data will be collected before, during, and after each breathing awareness/control exercise. Quantifying change in pain intensity has been demonstrated by pain threshold comparison across a stimulus using thermal Quantitative Sensory Testing (tQST). Functional near-infrared spectroscopy (fNIRS) in coordination with pain stimulation has been shown effective at locating different hemodynamic cortical responses depending on pain perception and expectation. In the current study, functional resting states before and after pain stimulation will be quantitatively assessed using fNIRS. The study design will allow the investigators to determine if the use of auditory and visual (3D imaging) stimuli related to the regulation of breathing can decrease or modulate pain. Cortical responses will give additional insight into the areas related to the decreased pain threshold. The long term objective is to increase neurophysiological understanding that will improve patient care. If effective, the novel experimental methods used will help to standardize future pain evaluation techniques.

NCT ID: NCT04280796 Completed - Low Back Pain Clinical Trials

Changes in Affective Pain Processing in Human Volunteers

Start date: September 21, 2020
Phase: N/A
Study type: Interventional

The experience of pain is more than the conscious perception of nociceptive signals. Emotional and motivational aspects accompany pain, leading to its aversiveness and motivation for avoidance. In chronic pain, a negative hedonic shift has been proposed that is characterized by disproportionally increased emotional-motivational compared to sensory-discriminative pain responses. Such a negative hedonic shift is, for example, mirrored in very high comorbidity rates of chronic pain and affective disorders such as depression and anxiety. The aim of this study is to develop methods that allow the differentiation of sensory-discriminative and emotional-motivational pain response and to characterize mechanisms of the negative hedonic shift.

NCT ID: NCT04274673 Recruiting - Clinical trials for Chronic Pain, Acute Pain, Cotinine, Hysterectomy

The Correlation Between Cotinine and Postoperative Acute and Chronic Pain After Hysterectomy

Start date: December 1, 2019
Phase: Phase 4
Study type: Interventional

It is known that there is an association between smoking and acute/chronic pain. But it is so difficult to assess this relation with asking questions to the patients in the preoperative period. Because of that we want to measure the levels of the cotinine in the urine and later assess the correlation with acute and chronic pain in hysterectomy patients.

NCT ID: NCT04274530 Recruiting - Pain, Postoperative Clinical Trials

Cognitive Behavioural Therapy to Optimize Post-Operative Recovery Trial

COPE
Start date: January 25, 2021
Phase: N/A
Study type: Interventional

Psychological factors such as stress, distress, anxiety, depression, and poor coping strategies may be associated with ongoing pain following injuries such as fractures. To study this relationship, patients will undergo cognitive behavioural therapy (CBT) which is designed to modify such thoughts with the goal of reducing ongoing pain and improving quality of life. The goal of this study is to determine if CBT, versus usual care, reduces the prevalence of moderate to severe persistent post-surgical pain (PPSP) over 12-months post-fracture in patients with an open or closed fracture of the appendicular skeleton, treated with internal fixation.

NCT ID: NCT04271917 Completed - Pain, Acute Clinical Trials

Analgesic Effects of Cannabidiol for Simple Tooth Extractions in Dental Patients

SWAP
Start date: February 24, 2020
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the analgesic effects of cannabidiol for patients who have undergone simple tooth extraction. Participants will be randomized to one of four arms: treatment-as-usual (TAU), cannabidiol 17mg/mL, cannabidiol 37mg/mL, or placebo.

NCT ID: NCT04262362 Recruiting - Pain, Acute Clinical Trials

The Frequency Of Sodium Hypochlorite Extrusion During Endodontic Treatments

Start date: December 5, 2019
Phase:
Study type: Observational

Sodium hypochlorite is a commonly used irrigation agent. However, the solution may extrude beyond the apex of tooth and cause pain during the treatment.The aim of this prospective observational investigation is to determinate the frequency of the extrusion of sodtium hypochlorite in endodontically treated teeth.

NCT ID: NCT04259645 Completed - Acute Pain Clinical Trials

Volume Versus Concentration: Clinical Effectiveness of Single Shot Quadrates Lumborum Block Using Either a High Volume/Low Concentration or Low Volume/High Concentration Injectate for Total Hip Arthroplasty.

Start date: April 1, 2021
Phase: Phase 4
Study type: Interventional

There is Controversy about what is more critical volume or concentration to achieve an optimum analgesic treatment with quadratus lumborum block. From the experiences of the authors, the regular dose of 20 ml of Bupivacaine at 0.375% concentration could not be enough in some cases to produce an optimum analgesic treatment, especially in hip arthroplasties. What is proposed in this study is to evaluate whether the volume injected in the quadratus lumborum block is more important than the concentration of the local anesthetic in terms of control of pain during the next 24 hours after surgery and opioid consumption.

NCT ID: NCT04252833 Completed - Surgery Clinical Trials

Open-label, Crossover, Food Effect Study to Evaluate CT-044 in Healthy Human Volunteers

Start date: February 18, 2020
Phase: Phase 1
Study type: Interventional

This open-label study will be conducted to assess the bioavailability and PK of oral single doses of CT-044 following administration with and without food and to evaluate the safety and tolerability of CT-044 when given with and without food.

NCT ID: NCT04251819 Active, not recruiting - Analgesia Clinical Trials

Buprenorphine Plus Baclofen to Increase Analgesia in Healthy Volunteers

Start date: January 21, 2021
Phase: Phase 2/Phase 3
Study type: Interventional

To determine if baclofen will enhance buprenorphine analgesia for acute pain in healthy volunteers.