The Efficacy of Enteral Nutrition in Fill of the Treatment Blank Period of the Postoperative Maintain Remission Medication for Crohn's Disease (CD)

Crohn's Disease Clinical Trial

Official title:

A Randomized, Controlled, Open-label Study to Assess the the Efficacy of Enteral Nutrition in Fill of the Treatment Blank Period of the Postoperative Maintain Remission Medication for Crohn's Disease (CD).

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT01823042
• Other study ID #: CDS-2
• Status: Recruiting
• Phase: N/A
• First received: March 25, 2013
• Last updated: March 28, 2013
• Start date: October 2012
• Est. completion date: July 2013

Study information

• Verified date: March 2013
• Source: Jinling Hospital, China
• Contact: n/a
• Is FDA regulated: No
• Health authority: China: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

Crohn's disease(CD) is a agnogenic disease which has a lifelong relapse tendency even after surgery treatment.So maintain remission medications were routinely given to patients after surgery.But maintain remission medications,as azathioprine,6-MP, ciclosporin,tripterygium glycosides, had a onset time.The therapeutic effect may appear 3 months~6months after taken medicine.There is a treatment blank period between surgery and onset time of maintain remission medications.Enteral nutrition has been used in the induction remission and maintain remission for CD.May be it can fill the treatment blank period.

Description:

Crohn's disease(CD) is a agnogenic disease which has a lifelong relapse tendency even after surgery treatment.So maintain remission medications were routinely given to patients after surgery.But maintain remission medications,as azathioprine,6-MP, ciclosporin,tripterygium glycosides, had a onset time.The therapeutic effect may appear 3 months~6months after taken medicine.There is a treatment blank period between surgery and onset time of maintain remission medications.Enteral nutrition has been used in the induction remission and maintain remission for CD.May be it can fill the treatment blank period.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 100
• Est. completion date: July 2013
• Est. primary completion date: July 2013
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• Subjects should have a definitive diagnosis of Crohn's disease, based on WHO criteria

• Subjects having curative resection/ileocolonic anastomosis,pathologically diagnosed as Crohn's disease

• Lesions located in ileum or ileocecal region

• Males and females = 18 years old, including women who are not pregnant or lactating at the time of enrollment.

• Body weight between 40 and 100 kg, inclusive.

• Subjects should have a CDAI score <150 at week 0

• Able to swallow tablets

• Are capable of providing written informed consent and obtained at the time of enrollment

• Willing to adhere to the study visit schedule and other protocol requirements.

Exclusion Criteria:

• Bacterial,viral or other microbial infection(including HIV)

• any of the following medications taken within 12 weeks before surgery: cyclosporine, tacrolimus, sirolimus, mycophenolate mofetil, or other investigational drugs

• any of ongoing therapy for Crohn's disease with: 5-ASA compounds, steroids, immune modifiers, systemic antibiotics, and tube feeding

• Needing orally administered corticosteroids for the treatment of other diseases. Inhaled or dermatologic preparations are acceptable.

• Previous or current use of infliximab.

• current use of prescription doses or chronic/frequent use of NSAIDs

• Treatment with narcotic pain medications. (Anti-diarrheal agents such as loperamide and diphenoxylate are permitted, providing that the dose is not increased during the study period.)

• History of pancreatitis, except for subjects with a known but removed cause(such as gallstone pancreatitis)

• WBC <3.0 x 109/L, hemoglobin <80 g/L, Platelets<50,000/mm3 at the time of enrollment (or within the previous 6 months, if known)

• History of abnormal liver function tests, including AST or ALT >1.5 times upper limit of normal, alkaline phosphatase >2 times upper limit of normal, total bilirubin >2.5 mg/dL at screening (or within the previous 6 months, if known)

• With short bowel syndrome (defined as requiring oral or parenteral supplemental or total nutrition to maintain stable body weight, or more than 100 cm of small bowel resected)

• History of malignancy

• Women who are pregnant or lactating at the time of enrollment, or who intend to be during the study period.

• Participation in other clinical trial within the past 6 months

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Crohn Disease
• Crohn's Disease

Intervention

Drug:
• azathioprine+enteral nutrition

• Azathioprine

Locations

Country	Name	City	State
China	General Surgery Institute,Jinling Hospital	Nanjing	Jiangsu

Sponsors (1)

Lead Sponsor	Collaborator
Jinling Hospital, China

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The change of patients'CDAI.		at 0 week, the 4 weeks, the 8 weeks, the 12weeks	No
Primary	patients' endoscopic score(Rutgeerts score).		at the 12weeks	No
Secondary	The change of haematological inflammation marker(CRP,ESR)		at 0 week, the 4 weeks, the 8 weeks, the 12weeks	No
Secondary	The change of patients'IBDQ.		at 2 week, the 6 weeks, the 12 weeks	No
Secondary	The change of blood routine examination and blood biochemistry.		at 0 week,4 weeks,8 weeks,12 weeks	No