Montreal General Hospital
Montreal, Quebec, H3G1A4, Canada
NCT Number: NCT01424254
The study objective is to compare the cost-effectiveness of VCE to push enteroscopy in patients with gastrointestinal bleeding of obscure origin with a negative initial work-up.
Looking for future studies?
Notify Me18 year and older
All sexes
Interventional
Phase 3
Montreal, Quebec, H3G1A4, Canada
Background: The introduction of the wireless capsule endoscopy (WCE) may dramatically alter the management of patients with small bowel disease such as chronic gastrointestinal bleeding of obscure origin (CGB). Yet, to date, this non invasive technique has undergone widespread diffusion in the absence of properly designed prospective comparative cost-effectiveness evaluations.
Objectives: To examine the clinical impact and cost-effectiveness of a novel approach employing WCE compared to that of push enteroscopy (PE).
Hypothesis: WCE is more cost-effective than PE in patients with CGB. Study design: We propose a randomized clinical trial comparing WCE to PE. Study population: Patients with CGB having undergone initial normal assessment with gastroscopy, colonoscopy and radiological examination of the small bowel.
Outcomes: Primary objective: To compare the detection rates of "clinically significant" small bowel lesions using WCE versus PE in CGB patients randomized to either modality. Secondary objectives: To determine the "cure rate" for each technique after 6 months, the cost-effectiveness of WCE versus PE, the type of small bowel lesions most likely to impact on clinical care, inter-rater variability in reading WCE examinations, the feasibility of WCE interpretation by a dedicated technician, the safety of each imaging modality, and to compare patient satisfaction and quality of life between the two groups.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Injection of Capsule Endoscopy
currently recommended standard
Time frame: 12 months
Time frame: 12 months
Time frame: 12 months
Time frame: 12 months
Time frame: 12 months
Time frame: 12 months
Time frame: Following procedure at randomization
Patient satisfaction questionnaire
McGill University Health Centre/Research Institute of the McGill University Health Centre
Other
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT02467621
Bacterial Infections, Bacterial Infections and Mycoses
Aalborg, Denmark
View Trial DetailsNCT03540368
Digestive System Diseases, Gastrointestinal Bleeding
Jakarta Pusat, DKI Jakarta, Indonesia
View Trial DetailsNCT06441201
Digestive System Diseases, Gastrointestinal Bleeding
Rochester, Minnesota, United States
View Trial DetailsNCT07025941
Acute Kidney Injury, Acute Kidney Injury (AKI)
Taizhou, Jiangsu, China
View Trial Details