Status:
COMPLETED
Evaluation of Colonoscopy With a Specific Device for the Detection of Adenomas
Lead Sponsor:
Dr. Alberto Herreros de Tejada Echanojáuregui
Collaborating Sponsors:
Spanish Clinical Research Network - SCReN
Conditions:
Colorectal Cancer
Adenoma Colon
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
Evaluation of colonoscopy with a specific device for the detection of adenomas: Multicenter, prospective and randomized study
Detailed Description
Given the discrepancy in the results of the published studies, the main objective of the present study would be to evaluate, through a multicentric design and with a sufficiently large sample of patie...
Eligibility Criteria
Inclusion
- All patients must be adults (≥18 years), give their consent for endoscopic exploration, for the study and meet following inclusion criteria:
- Patients with positive immunologic fecal occult blood test (IFOBT) for population screening.
- Patients invited to an opportunistic screening colonoscopy or included regional population screening program.
- Patients with a family history of CRC and indication of screening colonoscopy.
- Patients with follow-up colonoscopy indication by personal history of adenomas.
Exclusion
- Patients with absolute contraindications for colonoscopy (suspicion of intestinal obstruction or perforation, acute diverticulitis suspected or confirmed 6 weeks before the colonoscopy, etc).
- Symptomatic patients with indication of diagnostic colonoscopy.
- Patients with a personal history of CRC.
- Patients with a personal history of chronic inflammatory bowel disease (IBD).
- Patients with a known personal history of hereditary CRC syndrome:
- I. No polyposis (Lynch syndrome). II. Polypic.
- Patients with suspected attenuated polyposis (\> 20 adenomas) with genetic diagnosis not defined.
- Patients with total or partial colic resection.
- Complete colonoscopy with an adequate preparation (total Boston ≥6 with at least score ≥2 per segment) in a period of less than a year
- Pregnant or breastfeeding mothers.
- Patients who have expressed their wish not to participate or who do not have the ability to understand and / or sign informed consent.
- Patients with any serious and uncontrolled medical, psychological, psychiatric, geographic or social problem that could interfere with the participation of the patient in the study or not allow an adequate follow-up and adherence with the protocol and evaluation of the results of the study.
Key Trial Info
Start Date :
May 18 2018
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
June 4 2019
Estimated Enrollment :
1453 Patients enrolled
Trial Details
Trial ID
NCT03436004
Start Date
May 18 2018
End Date
June 4 2019
Last Update
August 22 2019
Active Locations (8)
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1
Department of Gastroenterology, Hospital Universitario Puerta de Hierro - Majadahonda
Majadahonda, Madrid, Spain, 28222
2
Department of Gastroenterology, Hospital Universitario La Princesa
Madrid, Spain, 28006
3
Department of Gastroenterology, Hospital General Universitario Gregorio Marañón
Madrid, Spain, 28007
4
Department of Gastroenterology, Hospital Universitario Ramón y Cajal
Madrid, Spain, 28034