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Behcet Syndrome clinical trials

View clinical trials related to Behcet Syndrome.

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NCT ID: NCT06276829 Completed - Behcet's Disease Clinical Trials

Behçet and LDH/Albumin

Start date: February 1, 2020
Phase:
Study type: Observational [Patient Registry]

ABSTRACT Objective: To investigate whether the lactate dehydrogenase to albumin ratio can be used as a parameter to determine disease severity in Behçet's disease, an inflammatory disease, by comparing it to healthy controls. Patients and Methods: In this retrospective cohort study, patients with Behçet's disease aged 18-69 years who presented to the outpatient clinic between February 2020 and April 2023 and healthy individuals of similar age and gender were enrolled. LDH, albumin levels, and LDH/albumin ratio of both groups were compared. Clinical findings and characteristics of Behçet's patients and disease severity were recorded and analyzed in relation to LDH/albumin ratio.

NCT ID: NCT05868538 Completed - Clinical trials for Behçet's Diseasecases

Calprotectin and Ischemia Modified Albumin Serum to Measure Disease Activity in Behçet's Disease

Start date: April 1, 2019
Phase:
Study type: Observational

Behçet's Disease activity was evaluated using BD Current Activity Form (BDCAF). Serum calprotectin and IMA concentrations were compared among active BD cases, inactive BD cases and control subjects.

NCT ID: NCT05142995 Completed - Behcet Syndrome Clinical Trials

Sleep Related Breathing Disorders, Anxiety, Depression and Quality of Life Assessment in Behcet's Disease

Start date: September 1, 2021
Phase:
Study type: Observational

Assessment of Sleep-related breathing disorders, anxiety, depression and quality of life in Behcet's disease.

NCT ID: NCT05098678 Completed - Behcet Syndrome Clinical Trials

Zinc Supplementation and Behçet's Syndrome

Start date: August 22, 2020
Phase: N/A
Study type: Interventional

To study the effects of zinc gluconate supplementation on patients with Behçet's syndrome, 50 patients will be randomly allocated to two groups: placebo group or zinc group (one tablet of 30 mg/day elemental zinc) for 12 weeks. All participants will be asked not to alter their diet, medication, and physical activity during the study. At the first and the end of the intervention, genes and proteins expression, the serum level of inflammatory factors, quality of life, disease activity, anthropometric measures, physical activity and serum level of zinc will be assessed and compared between groups.

NCT ID: NCT05032248 Completed - Behcet Syndrome Clinical Trials

Uses of Tacrolimus in Behcet Disease

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

Background: oral ulceration is the earliest and commonest manifestation of Behcet's disease (BD). Minor aphthous like ulcers (<10 mm in diameter) are the most common type (85%); major or herpetiform ulcers are less frequent. It is occurred about in Egypt; 3.6/100,000 % and high recurrence rate with traditional treatment. Colchicine is the first line of treatment in mucocutaneous manifestation of BD through its anti-inflammatory effect. Tacrolimus oral gel is safe and effective in treating aphthous ulcers in many diseases. Objectives: to compare the clinical efficacy of topical tacrolimus versus oral colchicine upon disease activity, pain and ulcer severity in oral ulcer associated with BD. Study design: A randomized double -blinded trial. Setting: Rheumatology clinic, Assiut University Hospital and Faculty of Dental Medicine, AlAzhar University, Assiut branch outpatient's clinic. Methods: 40 BD participants (> 3 months taken traditional treatment with persistent active oral ulceration). They have been equally randomized into either group I (Colchicine and topically applied Tacrolimus), or group II (Colchicine only). Measurements: Behcet's Disease Current Activity Form (BDCAF), Ulcer Severity Score (USS) and visual analog scale (VAS) pre-injection, then re-evaluated postinjection at four-time points (15 days, 1st, 2nd and 3rd months) and Determination of Natural Killer (NK) cells number in salival wash before treatment (at base line) and after the treatment (after 3 months)

NCT ID: NCT04961463 Completed - Nursing Caries Clinical Trials

Evaluation of the Psychoeducation Program Given to Behcet's Patients in the Context of the Roy Adaptation Model

Start date: September 15, 2016
Phase: N/A
Study type: Interventional

The physical, social and psychological effects of Behcet's disease necessitate the patient's adaptation in many areas. This study was conducted to examine the effect of psychoeducation given to Behcet's patients in the context of the Roy Adaptation Model on illness adjustment, dyadic adjustment, self-esteem, and psychiatric symptoms. The study is a control group quasi-experimental study with a pre-test, post-test and follow-up design. The study was conducted with 70 Behcet's patients including 35 interventions and 35 controls. The data of the study were collected using the "Patient Information Form", " Adaptation to Chronic Illness Scale", "Dyadic Adjustment Scale", "Rosenberg Self-Esteem Scale" and "Brief Symptom Inventory" in pre-test, post-test and follow-up measurements. A 7-session psychoeducation program was applied to the intervention group.

NCT ID: NCT04386824 Completed - Clinical trials for Erectile Dysfunction

Erectile Dysfunction in Patients With Non Ocular Behçet's Disease

Start date: June 15, 2019
Phase:
Study type: Observational

It was aimed to demonstrate whether erectile dysfunction is affected by BH pathogenesis and whether there is a relationship between erectile dysfunction and BD pathogenesis by assessing both sexual function and retinal micro-vascular blood flow in BH which may involve vessels from all calibrations and nature.

NCT ID: NCT04376411 Completed - Behcet Disease Clinical Trials

Role of Regulatory B Cells in Behçet's Disease

Start date: December 15, 2018
Phase:
Study type: Observational

There are limited data about the role of regulatory B cells in Behcet Disease. In this study we aimed to identify the proportions of total B lymphocytes and their regulatory subset in different Behcet Disease phenotype and therapies concentrating on the cardiovascular system attempting to unravel their function in Behcet Disease.

NCT ID: NCT04328064 Completed - Behcet's Disease Clinical Trials

The Role of Rosuvastatin on Vascular Involvement in Behçet's Disease

Start date: May 2010
Phase: N/A
Study type: Interventional

Behçet's Disease(BD) is a systemic inflammatory vasculitis, which affects all types and sizes of vessels. Statins display numerous effects often independent of the well-established lipid-lowering effects that may be of benefit in retarding or preventing vascular injury and ischaemic vascular events. The aim of the present study was to determine the efficacy of rosuvastatin in improving vascular dysfunction and vascular inflammation and to assess the effect of rosuvastatin on vascular involvement in BD patients. Fifty-six BD patients (51 males and 5 females) mean age 33.4 years, mean disease duration 5.8 years), all fulfilling the classification criteria of the International Study Group for Behçet's disease were recruited.Patients were randomised into 2 groups. The first group (n=27: 20 active and 7 inactive) were assigned to receive 40 mg of rosuvastatin and the second group(n=29: 21 active and 8 inactive) received placebo for 12 months. Inflammatory and endothelial dysregulation markers were measured at baseline and after 12 months. All patients were examined for vascular involvement. Venous or arterial system involvement was defined as present when confirmed by Doppler ultrasonography, magnetic resonance angiography, conventional angiography or CT.

NCT ID: NCT04065672 Completed - Behcet's Disease Clinical Trials

Low-dose IL-2 Treatment on Behcet's Disease

Start date: October 12, 2021
Phase: Phase 2
Study type: Interventional

The study aims to explore the clinical and immunological efficacy of low-dose IL-2 on Behcet's Disease.