To study the effect of an empirical treatment on idiopathic terminal ileitis
Phase 2
- Conditions
- Health Condition 1: K639- Disease of intestine, unspecified
- Registration Number
- CTRI/2020/02/023459
- Lead Sponsor
- OT APPLICABLE
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Age >18
Informed consent
Patients who showed terminal ileal ulcers (single or multiple) or nodularity as sole endoscopic abnormality
Exclusion Criteria
History of NSAIDs consumption ( <4 weeks)
History of colorectal surgery
History of tuberculosis
Oral or genital ulcerations
Recent history of intake of Angiotensin receptor blockers.
Coincidental ulceration in ileo-cecal valve or colon
Known case of inflammatory bowel disease
Recent history of gastroenteritis
Lymphoma
HIV
Previous ileal resection.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method