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Crohn's Disease clinical trials

View clinical trials related to Crohn's Disease.

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NCT ID: NCT02319798 Completed - Ulcerative Colitis Clinical Trials

Telephone Consultation as a Substitute for Routine Out-patient Face-to-face Consultation for Children With Inflammatory Bowel Disease

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

Inflammatory bowel disease (IBD) refers to two chronic diseases (Crohn's disease and ulcerative colitis) that affect the intestines. The number of new cases of IBD in people younger than 16 years old has been increasing in the United Kingdom (UK), and is currently estimated to be 700 new cases every year. There is no cure for IBD and patients experience episodes of flareups in between periods of wellbeing. Traditionally, children with IBD are asked to attend regular hospital appointments. This means that, even if they are well, they have to get to the hospital and this can involve travelling long distances. Telephone consultations have been shown to be beneficial in some areas of medicine but this approach has not been well studied in children. The aims of this study are to determine whether telephone consultations would improve quality of life, patient satisfaction, proportion of consultations attended and whether they would be safe and reduce costs for patients and the National Health Service (NHS). Investigators plan a randomised controlled trial involving 92 participants recruited from amongst the 250 children and adolescents aged between 8 and 16 years who attend the regional paediatric IBD centre in Manchester. Half will be assigned to telephone consultations, and half to face to face consultations. The study would have the approval of the local ethics committee and participants would have provided written consent. Investigators will compare outcomes in the two groups over 2 years. If telephone consultations prove to be effective, the NHS could offer children with IBD the choice of either telephone consultation or face to face consultation for their outpatient followup. Those who are doing well would not have to make unnecessary journeys to the hospital. This would free up clinic spaces and allow patients who are unwell, and new patients to be seen more quickly, thus reducing waiting

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: NCT02269358 Completed - Crohn's Disease Clinical Trials

Salvage Therapy With High/Low Methotrexate for Loss of Response to Infliximab Dose Escalation

Start date: July 2015
Phase: Phase 4
Study type: Interventional

The goal of the present study is to evaluate if addition of methotrexate can restore remission after loss of response to infliximab after dose escalation. another goal is to evaluate if low dose methotrexate can maintain remission achieved by regular dose methotrexate by 6 months.

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: NCT02256462 Completed - Crohn's Disease Clinical Trials

Pediatric Crohn's Disease AdalImumab Level-based Optimization Treatment (PAILOT) Trial

Start date: May 1, 2015
Phase: Phase 4
Study type: Interventional

Objectives: To examine the effect of drug level-based personalized treatment of adalimumab in children with Crohn's disease. Design: A prospective, randomized, open label study. Setting: Pediatric gastroenterology centers. Participants: Children 6 year to 17 years who are diagnosed with CD and are planned to receive adalimumab treatment. Main outcome measures: Pediatric Crohn's Activity Index (PCDAI) at 48 and 72 weeks. Secondary outcome measures: Corticosteroids free remission rates and on adalimumab at 48 and 72 weeks. The effect of routine adalimumab drug monitoring-based treatment on trough levels and anti-adalimumab antibodies during therapy.

NCT ID: NCT02255370 Completed - Crohn's Disease Clinical Trials

Curcumin Associated With Thiopurin in the Prevention of Post-op Recurrence in Crohn Disease

POPCUR
Start date: December 2014
Phase: Phase 3
Study type: Interventional

Curcumin, the active ingredient of turmeric, has been used for long term in the treatment of inflammatory conditions. Inhibition of NF-κB is postulated as the main mechanism responsible for the anti-inflammatory effect of curcumin Aim : to study the effect of curcumin, 3g per day, as compared to placebo, combined with thiopurines in the prevention of Crohn's disease post-operative recurrence.

NCT ID: NCT02233062 Completed - Crohn's Disease Clinical Trials

Impact of Exclusive Enteral Nutrition Therapy on Sperm Quality of Patients With Crohn's Disease

Start date: May 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate the impact of enteral nutrition therapy on sperm quality of patients with crohn's disease.

NCT ID: NCT02231814 Completed - Crohn's Disease Clinical Trials

The Crohn's Disease Exclusion Diet With Partial Enteral Nutrition or Alone in Adult Patients With Crohn's Disease

CDED-AD
Start date: December 2016
Phase: N/A
Study type: Interventional

This study will evaluate a novel diet for adult crohn's disease patients (The Crohn's Disease Exclusion Diet - CDED). Half of the patients in this study will receive the CDED alone while the other half will receive the CDED and a liquid diet formula, for 24 weeks.

NCT ID: NCT02213835 Completed - Ulcerative Colitis Clinical Trials

Treatment With the Specific Carbohydrate Diet for Children With Active Crohns Disease and Ulcerative Colitis

SCD
Start date: June 2014
Phase: N/A
Study type: Interventional

The aim of this study is to determine the tolerability and potential efficacy of dietary therapy, the Specific Carbohydrate Diet (SCD), in pediatric patients with Crohn's disease (CD) and Ulcerative Colitis (UC). This is a single center, open labelled study designed to determine tolerability, preliminary safety and potential efficacy in pediatric patients with CD and UC. The study patients will be recruited from Seattle Children's GI clinic. the investigators will enroll 10 patients with mild to moderate CD (defined as PCDAI score of 10-29) or Ulcerative colitis (PUCAI 10-60) ages 8 to 21 years. Each patient will be in the study for approximately 12 weeks.

NCT ID: NCT02201693 Completed - Crohn's Disease Clinical Trials

Cyclic Exclusive Enteral Nutrition as Maintenance Therapy for Pediatric Crohn's Disease

CD-HOPE
Start date: December 12, 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the rate of first relapse at 12 months between maintenance therapy with cyclic exclusive enteral nutrition (EEN) (at least 100% daily calories) and maintenance therapy with supplementary enteral nutritional support (25% daily calories).