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Pain Syndrome clinical trials

View clinical trials related to Pain Syndrome.

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NCT ID: NCT04625504 Completed - Chronic Pain Clinical Trials

Investigating Biological Targets, Markers, and Intervention for Chronic Pain

Start date: November 25, 2020
Phase: N/A
Study type: Interventional

This multi-modal methods study will investigate neurophysiological, endocrinological, cognitive, psycho-social-emotional markers of chronic pain, and therapeutic targets using integrative health treatments.

NCT ID: NCT04623827 Completed - Fibromyalgia Clinical Trials

Retrospective Study of Psychoattitudinal Patterns in Patients With Fibromyalgia Receiving Antalgic Therapy

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

Fibromyalgia (FM) is a widespread and invalidating disease that requires a multidisciplinary approach. Particularly, the psychiatric component seems to influence the algological management of these patients. Since January 2018, the HADS, SF-36, IMSA, TCI psycho-attitudinal questionnaires have been introduced in the Pain Therapy unit of Policlinico Sant'Orsola-Malpighi in an attempt to improve the care of patients diagnosed with FM. The aim of the study is to identify, through retrospective evaluation of TCI tests and its subdomains, compiled by patients with FM diagnosis, Pain Avoidance and Pain Persistance personality patterns, indicated in the literature. Anxiety and Depression incidence is also observed through retrospective evaluation of HADS tests. Patients in the Antalgic Therapy Outpatient Clinic diagnosed with FM, aged ≥18 years, who have completed selfadministered psychoattitudinal tests from January 2018 to January 2019 were considered. The data were collected in aggregate and extrapolated anonymously.

NCT ID: NCT04603274 Completed - Pain Clinical Trials

Efficacy of Electroacupuncture in Carpal Tunnel Syndrome

Start date: July 1, 2020
Phase: N/A
Study type: Interventional

The aim of this clinical study is to assess the effectiveness of electroacupuncture in reducing the severity of symptoms, in improving limb function, in improving the aesthetic and motor conduction of the median nerve and in reducing its cross-sectional area at the inlet of the carpal tunnel in patients with carpal tunnel syndrome. All upper extremities diagnosed with carpal tunnel syndrome will be treated with electroacupuncture for 8 sessions. Clinical, electrophysiological and ultrasonography outcome measures will be evaluated before and after the intervention, to assess the result.

NCT ID: NCT04587973 Completed - Anesthesia Clinical Trials

Bilateral Erector Spinae Plane Block (ESPB) in Laparoscopic Cholecystectomies

Start date: June 1, 2020
Phase: N/A
Study type: Interventional

The aim of the trial is to study the efficacy of bilateral Erector Spinae Plane Block (ESPB) in managing perioperative pain in patients who undergo elective laparoscopic cholecystectomy

NCT ID: NCT04586751 Completed - Breast Cancer Clinical Trials

The Impact of Pecs Blocks on Postmastectomy Pain Syndrome

Start date: August 1, 2020
Phase: N/A
Study type: Interventional

The aim of the present study is to investigate the incidence of chronic pain following breast cancer surgery in Cyprus, discover its associated risk factors and explore the impact of Pecs Blocks on the appearance of post mastectomy chronic pain symptoms

NCT ID: NCT04565600 Completed - Pain Syndrome Clinical Trials

Prevention of Taxane-associated Acute Pain Syndrome With Etoricoxib

Start date: March 1, 2020
Phase: Phase 2
Study type: Interventional

A phase II randomized clinical trial was conducted to determine whether etoricoxib could prevent or ameliorate the incidence and/or severity of docetaxel-induced acute pain syndrome. We also aimed to determine if there are any improvement of the late-onset peripheral neuropathy as well as quality of life with prophylactic etoricoxib for breast cancer patients who receive docetaxel chemotherapy.

NCT ID: NCT04555980 Completed - Pain Syndrome Clinical Trials

Warm Patch Decrease Propofol Injection Pain

Start date: March 20, 2020
Phase: N/A
Study type: Interventional

Propofol causes injection pain is still a common clinical unsolved problem. Mixing a small amount of lidocaine with propofol or injecting lidocaine in advance can reduce the pain caused by propofol injection. Using an air warmer to warm the arm can also reduce the pain caused by propofol injection. Investors suspect that treatment with a warming patch (covering the injection site) can also reduce the pain caused by propofol injection.

NCT ID: NCT04527770 Completed - Pain Syndrome Clinical Trials

Midazolam Versus Dexamethasone as an Adjuvant to Local Anesthetics in the Ultrasound Guided Hydrodissection of Median Nerve for Treatment of Carpal Tunnel Syndrome Patients

Start date: September 1, 2020
Phase: N/A
Study type: Interventional

midazolam and dexamethasone both can counteract chronic pain. either via GABA mimetic action or via anti prostaglandins

NCT ID: NCT04498923 Completed - Postoperative Pain Clinical Trials

Duration of Blockade of Peripheral Nerves With Bupivacaine Depending of the Adjuvants

DBBA
Start date: January 1, 2018
Phase:
Study type: Observational

The main aim of the investigator's study is to propose combination of local anesthetics and adjuvants that provides both adequate anesthesia during surgery and prolonged post-operative analgesia.

NCT ID: NCT03793790 Completed - Chronic Pain Clinical Trials

The Role of Learning in Nocebo Hyperalgesia

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

Nocebo effects are adverse effects induced by patients' expectations. Nocebo effects on pain may underlie several clinical conditions, such as chronic pain. These effects can be learned via classical conditioning mechanisms. In the lab, nocebo effects are commonly studied via conditioning with continuous reinforcement (CRF) during which 100 percent of unconditioned pain stimuli are paired to conditioned stimuli (i.e., the activation of a mock medical device). Partial reinforcement (PRF) provides a more uncertain pairing during conditioning, where less than 100 percent of unconditioned pain stimuli are paired to conditioned stimuli. This method provides a potentially more clinically relevant learning platform to study how nocebo effects on pain are induced. In this study, the efficacy of conditioning with PRF, CRF, and sham-conditioning in inducing nocebo effects on pain will be compared. Furthermore, a counterconditioning method will be compared to an extinction method for the attenuation of nocebo effects on pain. Given the relevance of nocebo effects for patients, it is important to ascertain effective & clinically relevant methods to understand how nocebo effects may be formed and attenuated. This study is conducted by Leiden University.