Enhanced Algorithm for Crohn's Treatment Incorporating Early Combination Therapy
- Conditions
- Crohn's Disease
- Interventions
- Other: Conventional Step-care AlgorithmOther: Enhanced Treatment Algorithm
- Registration Number
- NCT01698307
- Lead Sponsor
- Alimentiv Inc.
- Brief Summary
Assess if the implementation of an enhanced treatment algorithm will improve the management Crohn's Disease compared to a conventional Step-care approach.
- Detailed Description
Crohn's disease (CD) is a chronic inflammatory disorder of the gastrointestinal tract. During disease exacerbations, pharmacological or surgical intervention is usually needed to re-establish remission. Ideally, strategies should be employed to maintain patients in long-term remission while minimizing exposure to corticosteroids and reduce therapy-related toxicity.
Nevertheless, in reality many patients with CD do not receive effective therapy and their disease often remains active, leading to uncontrolled inflammation and complications from either the underlying disease or corticosteroids.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 1095
- Documented diagnosis of CD
- Written informed consent must be obtained and documented.
- Willing to utilize study supply of adalimumab provided in syringe format, if indicated according to treatment algorithm.
- Any conditions (e.g., history of alcohol or substance abuse) which, in the opinion of the investigator, may interfere with the patient's ability to comply with study procedures.
- Latex allergy or other conditions in which adalimumab syringes are contraindicated
- Currently participating, or planning to participate in a study involving investigational product within 24 months that may interfere with the patient's ability to comply with study procedures.
- Previously failed all classes of tumor necrosis factor (TNF) antagonists for the treatment of CD.
- Diagnosis of short bowel syndrome
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Conventional Step-care Algorithm Conventional Step-care Algorithm Step-care algorithm that specifies treatment escalation solely on the basis of symptoms quantified using the Harvey Bradshaw Index (HBI). Enhanced Treatment Algorithm Enhanced Treatment Algorithm The Enhanced algorithm features the early use of combined antimetabolite/adalimumab therapy, and treatment intensification based on ileocolonoscopic findings. Failure to achieve or sustain Deep Remission, which includes sustained normalization of the imaging studies, will result in treatment intensification, according to the steps outlined in the algorithm, irrespective of symptoms.
- Primary Outcome Measures
Name Time Method Risk of Crohn's Disease-related complications at two years 2 years Crohn''s Disease (CD)-related complications include (1) CD-related surgeries and non-surgical CD events (such as disease flare, bowel obstruction, and bowel damage events (such as symptomatic bowel obstruction, fistula, abscess and CD related hospitalizations and 2) complications and hospitalizations related to CD medications or procedures.
- Secondary Outcome Measures
Name Time Method Risk of Crohn's Disease-related complications, Crohn's Disease-related hospitalizations, and all cause hospitalizations at 6 months and 12 months. six months, 12 months Crohn's Disease (CD)-related complications include (1) CD-related surgeries and non-surgical CD events (such as disease flare, bowel obstruction, and bowel damage events (such as symptomatic bowel obstruction, fistula, abscess and CD related hospitalizations and 2) complications and hospitalizations related to CD medications or procedures.
Time to first Crohn's Disease-related complication, first Crohn's Disease-related hospitalizations, and first all cause hospitalizations at 6 months and 12 months. six months, 12 months Crohn's Disease (CD)-related complications include (1) CD-related surgeries and non-surgical CD events (such as disease flare, bowel obstruction, and bowel damage events (such as symptomatic bowel obstruction, fistula, abscess and CD related hospitalizations and 2) complications and hospitalizations related to CD medications or procedures.
Trial Locations
- Locations (22)
Oravec Medicine Professional Corporation
π¨π¦Oshawa, Ontario, Canada
Louisiana Research Center, LLC
πΊπΈShreveport, Louisiana, United States
Asheville Gastroenterology Associates, PA
πΊπΈAsheville, North Carolina, United States
The Royal Hampshire County Hospital
π¬π§Winchester, Hampshire, United Kingdom
Verein fur Wissenschaft und Fortbildung
π©πͺOldenburg, Lower Saxony, Germany
Sudbury Endoscopy Center
π¨π¦Sudbury, Ontario, Canada
The Office of Dr. Pierre Laflamme
π¨π¦Saint-Charles-BorromΓ©e, Quebec, Canada
Praxis fur Gastroenterologie am Bayerischen Platz
π©πͺBerlin, Germany
Oxford University Hospitals NHS Foundation - John Radcliffe Hospital
π¬π§Headington, Oxford, United Kingdom
University Hospital Coventry
π¬π§Coventry, West Midlands, United Kingdom
Royal Berkshire NHS Foundation Trust
π¬π§Reading, Berkshire, United Kingdom
Scott and White Memorial Hospital
πΊπΈTemple, Texas, United States
New Cross Hospital - Royal Wolverhampton NHS Trust
π¬π§Wolverhampton, West Midlands, United Kingdom
The Royal Bournemouth Hospital
π¬π§Bournemouth, Dorset, United Kingdom
Dr. Fashir Medical Inc.
π¨π¦Sydney, Nova Scotia, Canada
S. and T. Shulman Medicine Professional Corporation
π¨π¦North Bay, Ontario, Canada
Nottingham University Hospitals NHS Trust
π¬π§Nottingham, United Kingdom
Georgetown University Hospital
πΊπΈWashington, District of Columbia, United States
Gastroenterologie Eppendorfer Baum
π©πͺHamburg, Germany
The Office of Dr. Bruce Musgrave
π¨π¦Kentville, Nova Scotia, Canada
Carle Foundation Hospital
πΊπΈUrbana, Illinois, United States
Duane Sheppard, GI Inc.
π¨π¦Dartmouth, Nova Scotia, Canada