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NCT ID: NCT04364555 Recruiting - Oral Lichen Planus Clinical Trials

Efficacy of Topical Treatment With Clobetasol in Symptomatic Oral Lichen Planus.

Start date: May 18, 2020
Phase: Phase 2/Phase 3
Study type: Interventional

The investigators want to study the effect of clobetasol in symptomatic oral lichen planus. The investigators will include 90 patients and randomly allocate them in three groups. The first group will receive active treatment both in the morning an evening. Group two receives placebo in the morning and active treatment in the evening. Group three will get placebo both in the morning and in the evening. All Groups will follow the same protocol with rinsing twice daily with test substance in conjunction with antifungal treatment. The patients will be controlled after two weeks and and again after another two weeks. A biopsy will be performed at inclusion and another biopsy will be taken at the end of the test period. Smears for candida will also be evaluated. The patients will be examined for changes in clinical appearance and will answer questions to note changes in symptoms. Our hypotheses: #Patients receiving clobetasol will have a better resolution af symptoms than those who got placebo. #Patients treated with clobetasol twice daily will have a faster relief of symptoms than patients just treated once daily. #The clinical signs of oral lichen planus will diminish more pronounced in the two groups given active treatment. #A majority of the OLP lesions were infected by candida. #Specific histological changes can be seen in the biopsies taken after clobetasol treatment compared to those taken before treatment.

NCT ID: NCT04359628 Recruiting - Heart Failure Clinical Trials

How Does Patients' Overall Assessment of Their Health Vary Across and Within Different Disease Groups?

SWEQR
Start date: January 2002
Phase:
Study type: Observational [Patient Registry]

EQ-5D is one of the most commonly employed patient-reported outcome (PRO) measures. It is included in many of the Swedish National Quality Registers (NQRs). EQ-5D health states are usually summarized using 'values' obtained from healthy members of the general public. However an alternative - which remains to be studied in detail - is the potential to use patients' self-reported overall health on the visual analogue scale as a means of capturing experience-based values. The overall aim of this project is to increase knowledge on the potential applicability of EQ VAS as a health state valuation method through assessment of its variability across and within patient groups and compared with that of the general population in Sweden. Data on nearly 700,000 patients from 12 NQRs covering a variety of diseases/conditions and from the general population will be analysed. Longitudinal studies of PROs among different patient groups will be conducted at baseline/first visit and 1-year follow-up. Descriptive analyses comparing EQ-5D health states and observed self-assessed EQ VAS within and across registers will be performed. Comparisons of the change in health state and observed EQ VAS values over one year will also be made. Regression models will be used to assess whether EQ-5D dimensions predict observed EQ VAS values to investigate patient value sets in each NQR. These will be compared across the patient groups and with the existing Swedish experience-based VAS and time trade-off (TTO) value sets obtained from the general population. This research project will provide information on the variation among different patient groups in terms of self-reported health status through EQ VAS and comparison with the general population. Knowledge on the relative importance of different dimensions of the EQ-5D to different patient groups as well as the general population will be gained in this project. The possibility of getting value sets based on patients' self-reported EQ VAS values and their comparison with value sets from experience-based general population studies will be discussed.

NCT ID: NCT04358328 Recruiting - Clinical trials for Colorectal Neoplasms

Effect of CGA for Frail Elderly Patients Operated for Colorectal Cancer - The CRC Frailty-study

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

This multicentre randomized controlled trial aims to investigate whether an individualized comprehensive geriatric assessment (CGA) and care will improve postoperative results in frail elderly patients undergoing surgery for colorectal cancer. The study will take place in departments applying the ERAS-concept which is considered gold standard in colorectal surgery.

NCT ID: NCT04358159 Recruiting - Clinical trials for Incisional Hernia of Midline of Abdomen

RCT Ventralex vs Onlay Mesh in Incisional Hernias

VPatchIncRCT
Start date: January 1, 2021
Phase: N/A
Study type: Interventional

A radomised controlled trial comparing Ventralex patch and Progrip mesh in surgery for midline incisional hernias

NCT ID: NCT04356976 Recruiting - Ventral Hernia Clinical Trials

Ventralex vs Stratafix for Primary Ventral Hernias

VPatchPriRCT
Start date: January 1, 2021
Phase: N/A
Study type: Interventional

Randomised controlled trial comparing Ventralex Hernia Patch with Stratafix suture for repair of primary ventral hernias in the midline.

NCT ID: NCT04356924 Recruiting - Clinical trials for Cognitive Impairment

Psychological Treatment to Support the Consequences of Cognitive Impairment

Start date: September 7, 2023
Phase: N/A
Study type: Interventional

The burden of cognitive impairment is severe, and often hinders affected people to act independently in daily life. Individuals in different stages of cognitive decline are frequently affected by existential distress and associated health issues (such as stress symptoms, anxiety, and depression), as well as social avoidance due to the unclear prognosis. Although the need for psychological support is large, there is a lack of efficient individualized psychological treatments- and methods to maintain psychological health that sufficiently impact daily life and promote behavioral- and biological change. In keeping with that notion, the investigators have developed a novel psychological treatment manual focused on supporting individuals with early phase cognitive impairment. The treatment manual is centered on facilitating behavioral change in accordance with personal values and long-term goals even in the presence of negative experiences, as well as to promote meaningful life-style changes. Conceptually, the treatment manual has its basis in the cognitive behavioral therapy (CBT) tradition, but the investigators have strived to adapt the manual to suit a cognitively affected population. The investigators will evaluate the psychological treatment in a RCT were the investigators will include approximately 138 individuals in their early phases of cognitive decline and randomize them into either an experimental group (psychological treatment), an active control group (cognitive training), or a treatment as usual control group. Evaluations will be conducted with, psychological health measures, cognitive assessments, and with biological markers. The investigators hypothesize that in comparison with the control conditions, the response to psychological treatment will be associated with improved psychological health and improved cellular protection.

NCT ID: NCT04351178 Completed - Stroke Clinical Trials

F@ce 2.0 - Information and Communication Technology-based Rehabilitation Intervention After Stroke in Sweden

Start date: February 11, 2021
Phase: N/A
Study type: Interventional

The purpose of the present proposal is to implement and evaluate a new model for mobile phone supported and family-centred rehabilitation intervention (F@ce 2.0) with regard to functioning in activities in daily living and participation in everyday life among persons with stroke and their families in rural and urban areas in Sweden.

NCT ID: NCT04350255 Recruiting - Prospective Clinical Trials

A Register Based Prospective Study During Implementation of a New Cup

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

In a prospective register-based study, we aim to evaluate the implant survival, clinical outcomes and X-ray findings by following a cohort of patients operated with the Trident II cup.

NCT ID: NCT04350021 Completed - Chemotherapy Effect Clinical Trials

Effect of Low Dose Metronomic Chemotherapy in Metastatic Breast Cancer

METRO
Start date: March 1, 2019
Phase:
Study type: Observational

Low dose metronomic chemotherapy (LDMC) in patients with metastatic breast cancer (MBC) is used as a palliative regiment with the aim to prolong and improve quality of life. The effect of LDMC is not fully elucidated. The aim is to evaluate the effect of LDMC with Capecitabine and Cyclophosphamide (CX) and to discover new potential predictive markers and potential markers for monitoring treatment effect.

NCT ID: NCT04346524 Recruiting - Type 1 Diabetes Clinical Trials

SweMaMi DMI, Microbiome

Start date: April 1, 2020
Phase:
Study type: Observational

Dysbiosis is associated with an increased risk of preeclampsia during pregnancy. The microbiome differs between those with and without type 1 diabetes and the cause of type 1 diabetes has been associated with dysbiosis. Increased knowledge of the microbiome and its variation, depending on the state of health during pregnancies complicated with type 1 diabetes, could in the future lead to preventive care and treatments during these pregnancies.