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NCT ID: NCT04242576 Completed - Pain, Neck Clinical Trials

Evaluation of Nociceptive Processing in the Cervical Region

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

The main objective of this research is to asses the effectivity of action observation therapy, left/right discrimination and therapeutic exercise in the nociceptive processing of the cervical region.

NCT ID: NCT04242498 Completed - Clinical trials for Hidradenitis Suppurativa

A Study to Evaluate the Efficacy and Safety of Bimekizumab in Study Participants With Moderate to Severe Hidradenitis Suppurativa

BE HEARD II
Start date: March 2, 2020
Phase: Phase 3
Study type: Interventional

The purpose of the study is to evaluate the efficacy and safety of bimekizumab in study participants with moderate to severe hidradenitis suppurativa (HS)

NCT ID: NCT04242446 Completed - Clinical trials for Hidradenitis Suppurativa

A Study to Evaluate the Efficacy and Safety of Bimekizumab in Study Participants With Moderate to Severe Hidradenitis Suppurativa

BE HEARD I
Start date: February 19, 2020
Phase: Phase 3
Study type: Interventional

The purpose of the study is to evaluate the efficacy and safety of bimekizumab in study participants with moderate to severe hidradenitis suppurativa (HS)

NCT ID: NCT04241978 Completed - Osteoarthritis Clinical Trials

Development and Evaluation of a Web Based Decision Aid for Patients With Hip Osteoarthritis

Start date: February 17, 2020
Phase: N/A
Study type: Interventional

The main goal of this study is assess the effectiveness of a PtDA for patients with hip osteoarthritis

NCT ID: NCT04241406 Completed - Motor Activity Clinical Trials

Transcutaneous Spinal Cord Stimulation in Healthy Subjects to Activate Central Pattern Generator

Start date: January 30, 2019
Phase: N/A
Study type: Interventional

The purpose of this study is to determinate whether the application of transcutaneous spinal cord stimulation produce changes in the excitability of alpha moto neurone in healthy volunteers. Moreover evidence whether the effect of the electric currents can increase muscle strength.

NCT ID: NCT04240106 Completed - Breast Cancer Clinical Trials

Niraparib Plus Aromatase Inhibitors for Luminal-like(HER2-,ER+) and gBRCA or HDR+ Metastatic Breast Cancer (LUZERN)

LUZERN
Start date: June 15, 2020
Phase: Phase 2
Study type: Interventional

This study evalues the efficacy -as determined by the clinical benefit rate (CBR)- of niraparib in combination with AIs in unresectable locally advanced or metastatic HR-positive/HER2-negative breast cancer patients harboring either gBRCAms or gBRCAwt and HRD. The planned number of patients is 23. Investigational product is Niraparib and will be administered daily continuously in 28-day cycles plus aromatase Inhibitors. Total study duration is 36 months and until 5 years of follow up.

NCT ID: NCT04238325 Completed - Clinical trials for General Population, no Specific Condition

Spanish Validation Frustration Discomfort Scale

Start date: January 10, 2020
Phase:
Study type: Observational

This is an observational study aimed at validating the Frustration Discomfort Scale (Harrington, 2005). A back-translation process was followed to obtain a translated version of the scale, which was refined after a discussion with several clinicians.

NCT ID: NCT04238286 Completed - Chronic Pain Clinical Trials

Influence of Catastrophism in Fibromyalgia Patients Following Dry Needling Treatment

Start date: January 7, 2020
Phase: N/A
Study type: Interventional

Background: Dry needling trigger point treatment, while painful, has been demonstrated as a useful tool in fibromyalgia patients for decreasing pain and central sensitization. However, the current biopsychosocial pain paradigm indicates that fibromyalgia subjects with high levels of catastrophizing have negative thoughts related with perceived partner responses to pain, which results in an emotional and physical stress after a painful episode. Objective: To assess whether catastrophizing could influence the perception of pain during and after dry needling application. Study design: A singled-blind randomized controlled trial. Setting: Department of Medicine, Faculty of Health Sciences, Universitat Jaume I Methods: Female fibromyalgia patients and number and age-matched female controls will be recruited and randomly assigned to either a real or a simulated dry needling group. The Spanish version of the pain catastrophizing scale will be used to assess the catastrophizing level of each participant before initiating any of the planned interventions. The perceived pain during and immediately after the dry needling procedure will be measured using the pain visual analogue scale, [VAS].

NCT ID: NCT04238156 Completed - Abdominal Diastasis Clinical Trials

Hypopressive Abdominal Exercise in Postpartum Abdominal Diastasis

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

The prevalence of abdominal diastasis is high in postpartum. The abdominal diastasis can impair the body posture, the of lumbo-pelvic stability and movement, or breathing. Exercises focused on the transversus abdominis muscle have been proposed as a therapeutic approach for abdominal diastasis. Hypopressive abdominal exercises have been used for postpartum recovery, for specific pathologies related to pregnancy (low back pain, pelvic floor dysfunction ...) and even for the rehabilitation of spinal pathologies. However, there is a lack of studies that determine its effectiveness and clinical utility. The aim of the study will be to analyze the effects of Hypopressive abdominal exercises on postpartum abdominal diastasis, the tone of the transverse abdominal muscle and the pelvic floor musculature. A case series design will be applied, with weekly assessment of the outcomes after the intervention and two months after the intervention.

NCT ID: NCT04236856 Completed - Headache Clinical Trials

CorPath® GRX Neuro Study

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

The primary objective of this study is to evaluate the effectiveness and safety of robotic-assisted endovascular embolization procedures compared to objective performance criteria for traditional, manual operation based on the scientific literature.