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Ulcer clinical trials

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NCT ID: NCT02280629 Completed - Ulcerative Colitis Clinical Trials

Phosphatidylcholine (LT-02) vs. Placebo vs. Mesalamine for Maintenance of Remission in Ulcerative Colitis (PROTECT-2)

PROTECT-2
Start date: October 1, 2014
Phase: Phase 3
Study type: Interventional

The purpose of this study is to prove the superiority of a 48-weeks treatment with 3.2 g/day delayed-release phosphatidylcholine (LT-02) versus placebo for the maintenance of remission in patients with ulcerative colitis (UC)

NCT ID: NCT02277470 Recruiting - Ulcerative Colitis Clinical Trials

Study of the Pharmacokinetics of Golimumab in Moderate to Severe Ulcerative Colitis

GO-KINETIC
Start date: August 2014
Phase: N/A
Study type: Observational

The purpose of this study is to gain insights in the pharmacokinetics of golimumab in moderate to severe Ulcerative Colitis after subcutaneous administration, during induction and maintenance treatment the investigators will collect blood and stool samples at different time points.

NCT ID: NCT02277223 Withdrawn - Ulcerative Colitis Clinical Trials

Curcumin in Pediatric Ulcerative Colitis

Start date: March 1, 2020
Phase: Phase 3
Study type: Interventional

Background: Curcumin in an active phytochemical substance, used as part of the human diet, that has anti-inflammatory and anti-oxidative properties which were demonstrated in multiple experimental models of colitis including a positive effect on maintenance of remission in adult ulcerative colitis (UC) patients. Objectives: To examine the effect of curcumin as complementary medication in induction and maintenance therapy in pediatric patients with mild to moderate ulcerative colitis. Design: A prospective, randomized, placebo-controlled study. Setting: Pediatric gastroenterology centers. Participants: Children 6 year to 18 years who are diagnosed with mild to moderate UC and are planned to receive either 5-ASA or corticosteroids induction treatment. Main outcome measures: Disease activity defined by the Pediatric Ulcerative Colitis Activity Index (PUCAI) at 2 weeks and 6 months. Secondary outcome measures: Effect of curcumin treatment on serum inflammatory markers, calprotectin and fecal microbiota. Data analysis: Data will be collected and analyzed using SPSS (version 21.0, SPSS, Inc., Chicago, IL, USA). Fisher's exact test will be used to explore univariate associations between primary outcomes and categorical variables. Associations of continues variables with primary outcome measures will be examined using ANOVA with repeated measures. P-values <0.05 will be considered significant.

NCT ID: NCT02274714 Completed - Ulcerative Colitis Clinical Trials

Dysmenorrhea in Women With Crohn's Disease and Ulcerative Colitis

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

This case-control study will screen for dysmenorrhea and assess severity of menstrual symptoms in menstruating women with CD and UC compared with healthy age-matched controls. IBD activity will be characterized using previously validated clinical disease activity indices. General and health-related quality of life will be assessed using validated measures.

NCT ID: NCT02272881 Withdrawn - Pressure Ulcer Clinical Trials

A Randomized, Prospective Clinical Trial of Immediate Flap Closure Versus Wound Care for Management of Late-stage Pressure Ulcers

Start date: December 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the number of and degree of pressure ulcers healed, as measured by intact skin at the original ulcer site at 6 months of follow-up in patients randomized to immediate operative closure versus those who are maintained in a wound care program in patients with Stage 3 and 4 sacral and peri-sacral decubitus ulcers.

NCT ID: NCT02270385 Completed - Clinical trials for Prevention of Pressure Ulcers

The Effectiveness of a Pressure Ulcer Prevention Programme for Older People in For-profit Private Nursing Homes

Start date: November 2, 2015
Phase: N/A
Study type: Interventional

This study aims to evaluate the effectiveness of a PU prevention programme for for-profit private nursing homes

NCT ID: NCT02267694 Completed - Ulcerative Colitis Clinical Trials

Study of Freeze-dried Black Raspberry in Maintenance of Ulcerative Colitis

BRB
Start date: August 2013
Phase: Phase 1
Study type: Interventional

This research study is about adding Black Raspberry powder to the treatment regimen of patients with ulcerative colitis who are currently in remission and doing well.

NCT ID: NCT02265588 Completed - Depression Clinical Trials

Healthy Approach to Physical and Psychological Problems in Youngsters With IBD (HAPPY-IBD).

HAPPY-IBD
Start date: September 2014
Phase: N/A
Study type: Interventional

The presented study aims to reduce symptoms of depression and anxiety in adolescents with inflammatory bowel disease and increased symptoms of anxiety and depression by using the disease specific CBT program (PASCET-PI)in order to improve quality of life and to improve the clinical course of disease.

NCT ID: NCT02262169 Terminated - Clinical trials for Non-Bleeding Peptic Ulcers

DLBS2411 Treatment for Ulcer Healing in Non-Bleeding Peptic Ulcers

Start date: October 2014
Phase: Phase 3
Study type: Interventional

This is a 2-arm, prospective, double-blind, double-dummy, randomized-controlled study using DLBS2411 at a dose of 250 mg twice daily (before morning and evening meals), or omeprazole at a dose of 40 mg once daily (before morning meal), for an 8-week course of therapy, for the treatment of patients with any non-bleeding peptic ulcers. DLBS2411 is a bioactive fraction of an Indonesian native herbal, Cinnamomum burmanii, locally known as kayu manis have been proven at cellular and genetic levels to have an antiulcer effect through both suppressing the gastric acidity and enhancing gastric mucosal protection. The anti-secretory effect of DLBS2411 is exerted through the inhibition of H+/K+ ATPase 'pump' as well as down-regulation of the H+/K+ ATPase gene expression, thus suppressing gastric acid secretion; while its gastro-protective defense mechanism works through the promotion of COX-2 derived prostaglandin (PgE2) synthesis, stimulating gastric-epithelial mucous and bicarbonate secretion; anti-oxidative activity; and endothelial-nitric oxide (NO) formation. Recent study of DLBS2411 in healthy volunteers demonstrated the effective role and safety of DLBS2411 in suppressing intragastric acidity. Having such mechanisms of action, DLBS2411 is hypothesized to benefit in peptic ulcers.

NCT ID: NCT02261636 Completed - Ulcerative Colitis Clinical Trials

Induction and Maintenance of Remission With Pentasa as Ulcerative Colitis Treatment

IMPACT
Start date: January 2015
Phase:
Study type: Observational

For both induction of remission and in maintenance of remission, different doses and treatment durations are used in practice. The aim of this study is to assess how mesalazine is used in clinical practice, at which doses and for how long and how these differences impact the patient disease state and work productivity.