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Ulcer clinical trials

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NCT ID: NCT01353495 Completed - Clinical trials for Diabetic Foot Ulcers

Acellular Porcine Dermal Matrix Wound Dressing in the Management of Diabetic Foot Ulcers

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

Have indolent diabetic ulcers completely healed by the Acellular Porcine Dermal Matrix (APM) in 12 weeks.

NCT ID: NCT01353144 Completed - Peptic Ulcer Clinical Trials

A Comparison of Two Therapeutic Strategies for the Treatment of Aspirin-associated Peptic Ulcers

Start date: June 2007
Phase: Phase 4
Study type: Interventional

Esomeprazole plus aspirin compared with esomeprazole alone for the treatment of aspirin-related peptic ulcers.

NCT ID: NCT01348581 Completed - Pressure Ulcers Clinical Trials

Use of Fish Skin Extracellular Matrix (ECM) to Facilitate Chronic Wound Healing

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

The clinical study is designed to assess the effectiveness, safety and non-immunogenicity of fish skin wound dressing extracellular matrix (ECM) in treating chronic wounds. The wound dressing is indicated for the management of difficult to heal and chronic wounds. The matrix is cut to fit the wound and is applied to the wound bed. An absorptive secondary dressing is put on top. Further dressing of the wound depends on the etiology. The indications for use are: - partial and full-thickness wounds - pressure ulcers - venous ulcers - diabetic ulcers - chronic vascular ulcers - tunneled/undermined wounds - trauma wounds (abrasions, lacerations, second-degree burns, and skin tears)

NCT ID: NCT01346826 Completed - Ulcerative Colitis Clinical Trials

Safety of Accelerated Infliximab Infusions in Patients With Inflammatory Bowel Disease (IBD)

Start date: May 2011
Phase: Phase 4
Study type: Interventional

This study aims to test the hypothesis that the accelerated infusion of infliximab is not inferior to the conventional 2 hour infusion with respect to the frequency of infusion reaction.

NCT ID: NCT01340872 Completed - Ulcerative Colitis Clinical Trials

Safety and Efficacy Study of Oral Ferric Iron To Treat Iron Deficiency Anaemia in Quiescent Ulcerative Colitis (AEGIS-1)

AEGIS-1
Start date: August 2011
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether ST10-021, an oral ferric iron preparation, is safe and effective in the treatment of iron deficiency anaemia (IDA) in subjects with non-active ulcerative colitis (UC).

NCT ID: NCT01336465 Completed - Ulcerative Colitis Clinical Trials

Evaluate the Efficacy and Safety of rhuMAb Beta7 in Patients With Moderate to Severe Ulcerative Colitis

Start date: September 2011
Phase: Phase 2
Study type: Interventional

This Phase II study is a randomized, double-blind, placebo-controlled multicenter study to evaluate the efficacy and safety of rhuMAb Beta7 in patients with moderate to severe ulcerative colitis.

NCT ID: NCT01327937 Completed - Venous Ulcer Clinical Trials

A Post Marketing Study of Apligraf in Non-healing Wounds of Subjects With Venous Leg Ulcers

Start date: March 2011
Phase: Phase 4
Study type: Interventional

The overall study objective is to use microarray technology to identify and characterize the gene expression of multiple relevant genes in biopsies of non-healing venous ulcers.

NCT ID: NCT01320436 Completed - Ulcerative Colitis Clinical Trials

Curcumin + Aminosalicylic Acid (5ASA) Versus 5ASA Alone in the Treatment of Mild to Moderate Ulcerative Colitis

5ASA
Start date: July 2011
Phase: Phase 3
Study type: Interventional

Ulcerative colitis (UC) is a chronic inflammatory disease resulting in increased morbidity in patients. The current standard treatment for mild to moderate UC (MTMUC) includes 5-aminosalicylic compounds (5ASA) such as olsalazine and mesalamine, yet some patients continue to experience disease symptoms and flare-ups. These patients require higher dosages of 5ASA medications and in many cases escalate to steroid and/or immunosuppressant therapy which comprises higher risk of hazardous side effects. Curcumin, an active ingredient of the Indian herb Rhizoma Curcuma Longa, has been extensively studied in the context of inflammatory diseases. In humans, a controlled study using curcumin as an adjusted therapy to 5ASA medication has shown it to be superior to placebo in maintaining remission in MTMUC patients . A small, preliminary open label study has also shown efficacy in reducing disease symptoms and inflammatory markers in this group of patients . This data provides bases for investigating an integrative approach to optimize the current standard treatment in MTMUC patients. We speculate that using a combined therapy of 5ASA medication and curcumin could benefit this subgroup of patients and reduce morbidity and perhaps need for escalating pharmacological intervention.

NCT ID: NCT01320332 Completed - Ulcerative Colitis Clinical Trials

A Study of a Single Dose of ASP3291 in Subjects With Ulcerative Colitis

Start date: August 2010
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine the pharmacokinetics (PK) and to assess safety and tolerability of a single dose of ASP3291 in subjects with ulcerative colitis.

NCT ID: NCT01319123 Completed - Clinical trials for Moderatley to Highly Exuding Venous Leg Ulcers

Evaluate the Impact of Drawtex in Venous Leg Ulcers

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

This is a clinical study to comparatively evaluate the impact of Drawtex wound dressing against wound bioburden in moderately to highly exuding venous leg ulcers.