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Somatoform Disorders clinical trials

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NCT ID: NCT05318560 Not yet recruiting - Clinical trials for Myofascial Pain Syndrome

Efficacy of Local Anesthetic and Ozone Injection in Patients With Myofascial Pain Syndrome

Start date: June 30, 2022
Phase: N/A
Study type: Interventional

In this study, the investigators planned to compare local anesthetic injection added to stretching exercise, ozone injection treatment added to stretching exercise, and only stretching exercise in patients with upper trapezius muscle myofascial pain syndrome.

NCT ID: NCT05083897 Not yet recruiting - Clinical trials for Patellofemoral Pain Syndrome

Effect of Hip Adductors Isometric Contraction on Knee Extensors Isokinetic Torque in Patellofemoral Pain Syndrome

Start date: October 2021
Phase:
Study type: Observational

the study will be done to investigate the effect of hip adduction isometric contraction on the pain level by VAS and knee extensors peak torque by using the isokinetic dynamometer in patients with unilateral patellofemoral pain syndrome

NCT ID: NCT05022888 Not yet recruiting - Clinical trials for Myofascial Pain Syndrome

Near-Infrared Spectroscopy in Myofascial Pain Syndrome

Start date: August 23, 2021
Phase: N/A
Study type: Interventional

Myofascial pain syndrome is a regional pain syndrome accompanied by sensorial, motor and autonomic symptoms . myofascial trigger points are most frequently detected in the upper trapezius, levator scapula, and axial postural muscles such as rhomboid major. Myofascial pain syndrome is characterized by active myofascial trigger points in the form of focal hyperirritable nodules palpated in the tight band of the muscle . Alteration of tissue vascularization could limit or prevent th may cause adhesions, contractures and pain. As a result of decreased blood flow, tissue oxygenation may decrease.

NCT ID: NCT04989179 Not yet recruiting - Breast Cancer Clinical Trials

Incidence and Factors Affecting the Development and Outcome of Post Mastectomy Pain Syndrome

PMPS
Start date: August 2021
Phase:
Study type: Observational

Phase 1 of this multi-centre, prospective study aims to obtain a precise estimate of the local incidence of PMPS and identify biopsychosocial risk factors contributing to the development of PMPS. Recognition of the impact of PMPS on function and mood and quality of life in cancer survivors, and identification of risk factors would help physicians institute appropriate pre-operative counselling and preventive measures to reduce the development of PMPS. The investigators aim to follow up on the long-term multi-dimensional effects of PMPS, and continue to develop and validate a risk prediction model for patients at risk of PMPS in the next phase of the study.

NCT ID: NCT04528914 Not yet recruiting - Clinical trials for Functional Abdominal Pain Disorder

Low-FODMAP Diet for FAPD in Children.

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

This single-center, randomized, controlled, quadruple-blinded, superiority trial is performed to test the hypothesis that children with IBS and FAP-NOS who receive a low-FODMAP diet will have a lower mean abdominal pain intensity score compared with those who receive a regular diet after 4 weeks of intervention.

NCT ID: NCT04170166 Not yet recruiting - Clinical trials for Shoulder Subacromial Pain Syndrome

Subacromial Injections for Shoulder Subacromial Pain Syndrome - Anterolateral vs Posterior Approach

Start date: November 2019
Phase: N/A
Study type: Interventional

This study aims to determine if there is any difference in terms of pain relief in patients with shoulder subacromial pain syndrome, when given a steroid injection into the subacromial space via an anterolateral approach compared to a posterior approach.

NCT ID: NCT03825991 Not yet recruiting - Back Pain Clinical Trials

Psychiatric Comorbidity in Back Pain Disorders

Start date: July 1, 2019
Phase:
Study type: Observational [Patient Registry]

Introduction: Studies focusing on back pain do not compare different types of back pain diagnosis in relation to a specific psychiatric comorbidity, nor if the presence of psychiatric comorbidity affects treatment. There are limited knowledge on pharmacological treatment of back pain disorders,and especially if the presence of psychiatric comorbidity is an ad-on to the dosage of medication prescribed. Investigating the use of opioids and other pain medication in back patients and the potential effect of concomitant psychiatric comorbidity as well as taking psychiatric medication under consideration is therefore relevant. Aim: This aim of this PhD thesis is: 1) to estimate the prevalence of psychiatric comorbidity in patients with back pain disorders (BPD) compared to patients with no back pain. 2) Investigate if psychiatric comorbidity affects the type of treatment given. 3) Examine if the presence of psychiatric comorbidity affects the levels of pharmacological treatment given with a focus on both pain medication, such as opioids, as well as treatment with psychotropic medication. Methods:The association between back pain disorders and psychiatric comorbidity will be investigated using population-based registry data. The population will be defined as adult patients (+18) with a relevant back pain disorder using The National Danish Patient Registry. The following registries will be also utilized: A subdivision of the DNPR, the National Patient Registry - Psychiatry (NPD-Psych), The Danish National Prescription Database, The Danish National Health Service Register and the DREAM database. By using the Danish Civil Registry and the unique personal identification number assigned to all Danish citizens at birth, data across registries can be linked on an individual level. Ethics:The Region of Southern Denmark is the data controller for this project, and it is included in their records of personal data processing activities (file no. (18/3337).). Additional approvals or consents were not needed for this project based exclusively on national registries according to Danish law. The data processing was conducted according to EU and Danish legislation on processing of sensitive personal information and, as complies with internal regulations from the Region of Southern Denmark.

NCT ID: NCT03468491 Not yet recruiting - Clinical trials for Patellofemoral Pain Syndrome

The Additional Effect of Hallux Valgus Correction on Runners With First Ray Instability and Patellofemoral Pain Syndrome

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

The study purpose is to investigate the effectiveness of a program combining biomechanical taping with lower extremity neuromuscular exercises for runners with patellofemoral pain syndrome (PFPS) and hallux valgus

NCT ID: NCT03088215 Not yet recruiting - Fibromyalgia Clinical Trials

Shock-Waves to Treat Fibromyalgia Pain

SWPW-FPS
Start date: October 20, 2017
Phase: N/A
Study type: Interventional

Fibromyalgia pain syndrome is a common debilitating condition which associates mainly generalised pain, emotional distress and cognitive symptoms. The etiology is unknown, and no specific treatment exists so far. Lately, shock-waves have been used successfully to treat painful skeletal muscle, tendons and fascia, the investigators therefore hypothesize that shock-waves could be useful in alleviating Fibromyalgia pain. Two similar groups of participants bearing the condition will be prospectively compared. The first group will benefit from the application of shock-waves weekly for 12 weeks, the second will not. The investigators intend to study if there is any difference in pain and quality of life between the two groups at the end of the three months.

NCT ID: NCT01788176 Not yet recruiting - Clinical trials for Complex Regional Pain Syndromes

The Use of Zoledronic Acid to Complex Regional Pain Syndrome

Aclasta
Start date: December 2013
Phase: Phase 2
Study type: Interventional

To evaluate the efficacy and the safety of using a single, intravenous 5mg dose of zoledronic acid in managing pain in Complex Regional Pain Syndrome patients.