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Ulcer clinical trials

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NCT ID: NCT01729182 Completed - Gastric Ulcer Clinical Trials

Nexium Capsules LDA Specific Clinical Experience Investigation

Start date: January 1, 2013
Phase:
Study type: Observational

The purpose of this investigation is to collect following data in patients given Nexium capsule (Nexium) for long term in usual-post-marketing therapy to prevention of recurrence of gastric ulcer or duodenal ulcer with Low dose Aspirin (LDA).

NCT ID: NCT01694485 Completed - Ulcerative Colitis Clinical Trials

Abrilumab (AMG 181) in Adults With Moderate to Severe Ulcerative Colitis

Start date: November 16, 2012
Phase: Phase 2
Study type: Interventional

The primary objective of this study is to evaluate the effect of abrilumab on induction of remission in adults with moderate to severe ulcerative colitis after 8 weeks of treatment as assessed by a total Mayo Score ≤ 2 points, with no individual subscore > 1 point.

NCT ID: NCT01693133 Completed - Diabetic Foot Ulcer Clinical Trials

Trial of Dehydrated Human Amnion/Chorion Membrane (dHACM) In the Management of Diabetic Foot Ulcers

Start date: July 2012
Phase: N/A
Study type: Interventional

The objective of this study is to evaluate the percentage of patients with complete diabetic foot ulcer (DFU) closure following up to 12 weeks of treatment with either dehydrated human amnion/chorion membrane (dHACM) plus standard of care (SOC) or SOC alone.

NCT ID: NCT01692743 Completed - Ulcerative Colitis Clinical Trials

Telemedicine in Patients With Inflammatory Bowel Disease (TELE-IBD)

TELE-IBD
Start date: September 2012
Phase: Phase 3
Study type: Interventional

Improved methods are needed to monitor patients with inflammatory bowel disease. Telemedicine has shown promise in patients with other chronic diseases; pilot testing in our patients with inflammatory bowel disease demonstrated that the technology was feasible and improved clinical outcomes. The telemedicine system for patients with inflammatory bowel disease (Tele-IBD) should improve outcomes for patients, improve access to care in areas with limited resources, and decrease health care costs.

NCT ID: NCT01688258 Completed - Clinical trials for Genital Ulcer Disease (GUD)

New Multiplex Real-time PCR for Genital Ulcer Disease

Start date: January 2012
Phase: N/A
Study type: Observational

(i) To compare a new diagnostic PCR with established diagnostic procedures for T. pallidum (serology, dark field microscopy), H. ducreyi (cultivation), HSV types 1 and 2 (cultivation, PCR). (ii) To assess the frequency of infections with T. pallidum, H. ducreyi and HSV types 1 and 2 in patients with genital, anal and oropharyngeal ulcers by a new PCR.

NCT ID: NCT01684514 Completed - Colitis, Ulcerative Clinical Trials

Confocal Laser Endomicroscopy Findings in Patients With Proctosigmoiditis Before and After Initiation of Treatment

Start date: October 2012
Phase: N/A
Study type: Interventional

Confocal laser endomicroscopy (CLE) is a novel method in evaluation of microscopic structures in vivo. The examination is carried out with a confocal laser endomicroscope, which is either part of the endoscope (manufactured by Pentax) or probe based (manufactured by Cellvizio). Hereby, all parts of the gastrointestinal (GI) tract can be examined. The method has potential to replace conventional microscopy and the dynamic nature of the procedure allows visualization of structures and cellular processes in almost real-time. This provides us with a potentially new diagnostic tool with a promising future. To date only a few studies have been published on inflammatory bowel disease (IBD) and in the literature high-quality research is still lacking. The project consists of a blinded prospective observation and methodology study including inter- and intra-observation of patients with proctitis before and after initiation of local treatment. Hypothesis: CLE can be used to assess the degree and extend of acute and chronic inflammation and treatment response in patients with ulcerative colitis and is a sensitive supplementary to conventional diagnostics.

NCT ID: NCT01681160 Completed - Clinical trials for DIABETIC FOOT ULCERS

Study of Maggot Therapy in Diabetic Foot Ulcers

MDT
Start date: January 2009
Phase: N/A
Study type: Interventional

This study was a Kind of clinical trial with equal randomization, that have been done from January 2009 to June 2011 in the AFZALIPOOR hospital endocrine ward in Kerman-Iran on 128 diabetic patient who had foot wounds.Replacement of conventional therapy by new methodes is one of the more important aims for health professional specially for nurses.One of this new treatment is maggot therapy.

NCT ID: NCT01678300 Completed - Ulcerative Colitis Clinical Trials

Qualitative Study of Topical Mesalamine Adherence in Patients With Ulcerative Colitis(UC)

Start date: August 2012
Phase: N/A
Study type: Observational

The purpose of this protocol is: 1. To quantify the prevalence of adherence to topical mesalamine in patients with UC 2. To describe the determinants of medication adherence in patients with UC prescribed topical mesalamine

NCT ID: NCT01673412 Completed - Leg Ulcer Clinical Trials

Research of Prognostic Factors Associated With Healing of Venous Leg Ulcers

Start date: January 2003
Phase: N/A
Study type: Interventional

This study was undertaken to identify prospectively which clinical venous leg ulcer (VLU) characteristics known as possible prognostic markers, and which sociodemographic and psychologic factors associated with VLU are associated with complete healing at 24 weeks.

NCT ID: NCT01671748 Completed - Varicose Ulcer Clinical Trials

MIST Ultrasound Therapy Compared to United Kingdom Standard Care for the Treatment of Non-healing Venous Leg Ulcers

Start date: August 2012
Phase: N/A
Study type: Interventional

Chronic venous leg ulcers (VLUs) impact negatively on patients' quality of life. Standard treatment in the UK for patients with VLUs is compression bandaging or stockings. The MIST ultrasound system is a noncontact device which delivers low frequency ultrasound through a gentle saline mist directed at a patient's wound. This study aims to determine whether the use of the MIST device used in combination with standard treatments can improve healing of VLUs compared to UK standard practice. This will be assessed by measuring any reduction in wound size in the two groups after receiving 8 weeks of either Standard Care once a week or MIST combined with Standard Care three times a week.