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Active clinical trials for "Ulcer"

Results 1861-1870 of 2094

Peptic Ulcer Disease in Ischemic Heart Patients Taking Aspirin and Clopidogrel With or Without Proton...

Peptic UlcerUlcer Complications

Studies showed that combined use of clopidogrel and aspirin had a 25 % reduction of risk on myocardial infarction and stroke in patients who undergone percutaneous coronary intervention (PCI) when compared with use of aspirin alone. However, major GI bleeding rose in combined group than aspirin group. Use of proton pump inhibitor (PPI) which diminishes gastric acid secretion effectively reduces aspirin or clopidogrel associated ulcer or/and ulcer bleeding in general population and high risk patients. The investigator hypothesis is whether use of PPI can reduce ulcer and ulcer complication in patients taking both clopidogrel and aspirin.

Unknown status3 enrollment criteria

European Safety Registry in Ulcerative Colitis (P04808)

Ulcerative Colitis

This is a prospective, safety surveillance registry in participants with moderate-to-severe active ulcerative colitis (UC).

Completed12 enrollment criteria

Evaluating the Ease of Use of a VAC GranuFoam Bridge Dressing on Diabetic Foot Ulcers Receiving...

Diabetic Foot Ulcers

The study is aimed at evaluating the clinician's perceived ease of using the V.A.C. GranuForm bride dressing and the patients perceived level of comfort during the dressing wear.

Completed17 enrollment criteria

Envision® Surface Evaluation

Pressure Ulcer

This observational study will acquire initial clinical practice utilization and product safety data for the Envision® surface.

Completed2 enrollment criteria

The Avelle® Negative Pressure Wound Therapy System on Chronic Wounds

Diabetic Foot UlcerVenous Leg Ulcer

This study seeks to demonstrate the performance of Negative Pressure Wound Therapy on chronic wounds such as diabetic foot ulcers and venous leg ulcers. The primary objective of the study is to demonstrate the performance and safety of Avelle Negative Pressure Wound Therapy on wound and wound fluid management when used in accordance with the instructions for use. Participation in the study is anticipated to be two weeks. The Avelle™ NPWT System will be used for two weeks and participants will be seen for study visits during this time. Study participants will need to visit the doctor's office up to five times and, at a minimum, will be required to see the health care provider three times, dependent on the condition of the wound. Each visit is anticipated to last for approximately 45 to 60 minutes.

Completed26 enrollment criteria

Prognosis in UC After First Biological

Ulcerative Colitis

To study the long-term clinical outcome of patients with ulcerative colitis treated with first trial of biological therapy.

Completed2 enrollment criteria

Temporomandibular Dysfunction in Patients With Diabetic Foot Ulcers

Diabetic Foot UlcerTemporomandibular Disorder1 more

The aim of this observational study is to investigate the effects of the type, area and duration of ulceration on jaw pain, mandibular function limitation, TMD and swallowing in individuals with diabetic foot ulcers.The main questions it aims to answer are: Does the change in foot structure due to diabetic foot ulcer have an effect on the temporomandibular jointand swalloving? What are the determinants of tempomandibular dysfunction in individuals with diabetic foot ulcers? Participants (both groups) will be evaluated for quality of life, jaw functionality, mandibular dysfunction, oropharyngeal swallowing disorder, pain and diabetes complications.

Completed14 enrollment criteria

A Prospective Non-interventional Multicenter Study to Evaluate the Effectiveness of Adalimumab in...

Ulcerative Colitis

This is a prospective, single country, multi-center study in participants with ulcerative colitis (UC) treated with adalimumab. Up to 147 participants are enrolled at approximately 20 sites. The baseline assessment is performed prior to the first dose of adalimumab (Visit 1). Study visits are conducted at weeks 8, 16, 24, 32, 40, 48 and 56 after baseline in accordance with clinical practice. All participants will have one Follow-up for safety approximately 70 days after the last dose of adalimumab.

Completed8 enrollment criteria

Study of Clinical Course of Newly Diagnosed Moderate to Severe Ulcerative Colitis in Korea

ColitisUlcerative

The purpose of this study is to describe clinical course of newly diagnosed moderate to severe ulcerative colitis (chronic inflammatory disease of the colon) in tertiary referral hospitals in Korea for 5-year follow-up under usual care.

Completed8 enrollment criteria

Prevalence of Cytomegalovirus Infection in Patients With Quiescent Ulcerative Colitis

Ulcerative ColitisCytomegalovirus Infections

Colitis from reactivation of established cytomegalovirus (CMV) colonization can complicate the clinical course in patients with an acute flare of ulcerative colitis (UC). Accurate and timely detection of active CMV infection or disease with appropriate anti-viral therapy may reduce complications associated with acute UC flare. Limited information is available on the presence of colonic CMV infection in patients with quiescent ulcerative colitis. Prospective studies on factors associated with reactivation of CMV infection during active UC flare and its impact on disease progression are lacking. The hypothesis of this study are as follows: 1) CMV infection is prevalent in patients with ulcerative colitis irrespective of disease severity; 2) The degree of immunosuppression directly impacts CMV infection status in patients with ulcerative colitis

Completed10 enrollment criteria
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