Adenoma Clinical Trial
Official title:
A Repeated Instruction by Telephone on the Day Before Colonoscopy Improves the Quality of Bowel Preparation and Colonoscopy Procedure : a Prospective Randomized, Controlled Trial
Verified date | December 2013 |
Source | Fourth Military Medical University |
Contact | n/a |
Is FDA regulated | No |
Health authority | China: Food and Drug Administration |
Study type | Interventional |
Cell phone retell the instruction of bowel preparation on the day before colonoscopy would help patient to prepare for colonoscopy and improve the quality of the bowel preparation.
Status | Completed |
Enrollment | 605 |
Est. completion date | July 2012 |
Est. primary completion date | July 2012 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 18 Years to 75 Years |
Eligibility |
Inclusion Criteria: - patients undergoing colonoscopy Exclusion Criteria: - disturbance of water and electrolyte - history of colorectal surgery - severe colonic stricture or obstructing tumor - known or suspected bowel obstruction or perforation - toxic colitis or megacolon - dysphagia - compromised swallowing reflex or mental status - significant gastroparesis or gastric outlet obstruction or ileus - severe chronic renal failure (creatinine clearance <30 mL/minute) - severe congestive heart failure (New York Heart Association class III or IV) - uncontrolled hypertension (average systolic blood pressure >170 mm Hg, average diastolic blood pressure >100 mm Hg) - pregnant or lactating women - patients who cannot give informed consent |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Investigator, Outcomes Assessor), Primary Purpose: Screening
Country | Name | City | State |
---|---|---|---|
China | Endoscopic center, Xijing Hospital of Digestive Diseases | Xi'an | Shaanxi |
Lead Sponsor | Collaborator |
---|---|
Fourth Military Medical University |
China,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Adequate bowel preparation quality at the time of colonoscopy defined by Ottawa score<6 | Ottawa score:A)cleanliness of each part of the colon: 0=excellent 1=good 2=fair 3=poor 4=inadequate B)fluid in whole colon: small=0 moderate=1 large=2 The bowel preparation was considered inadequate if (1) inadequate visualization on colonoscopy defined by Ottawa score=6; (2) the colonoscopy was cancelled because of poor bowel preparation or personal reasons; (3) incomplete colonoscopy. |
up to 3 months | No |
Secondary | Cecum intubation time | Total time of colonoscope intubation from anus to cecum | up to 3 months | No |
Secondary | Withdrawal time | Total time of colonoscope intubation from cecum to anus | up to 3 months | No |
Secondary | Polyp detection rate | The proportion of participants with at least one polyp in each group | up to 3 months | No |
Secondary | Compliance rate to instruction | The proportion of participants compliance to instruction of bowel preparation | up to 3 months | No |
Secondary | Willingness undergo a repeated bowel preparation | The number of patients have a willingness to undergo a repeated bowel preparation if needed | up to 3 months | No |
Status | Clinical Trial | Phase | |
---|---|---|---|
Active, not recruiting |
NCT05551052 -
CRC Detection Reliable Assessment With Blood
|
||
Recruiting |
NCT02545699 -
Prospective Trial to Compare ADR of G-EYE™ Colonoscopy With Standard Colonoscopy
|
N/A | |
Completed |
NCT01802008 -
Comparison of Adenoma Detection Miss Rates at Colonoscopy Associated With Different Withdrawal Times
|
N/A | |
Recruiting |
NCT01211132 -
Cap Assisted Colonoscopy for the Detection of Colon Polyps
|
N/A | |
Completed |
NCT04287335 -
Multitarget Stool FIT-DNA Study for Colorectal Cancer Early Screening in China
|
||
Not yet recruiting |
NCT06398418 -
R-5780-01 In Combination With PD-1 Checkpoint Inhibitors (Checkpoint Protein on Immune Cells Called T Cells) in Patients With Solid Tumors
|
Phase 1 | |
Recruiting |
NCT05362344 -
Colorectal Cancer Screening in Cystic Fibrosis
|
||
Completed |
NCT03268200 -
The Effect of Segmental Re-examination of Colon for Adenoma Detection in Colonoscopy
|
N/A | |
Recruiting |
NCT04591145 -
Multi-center Validation of a Deep Learning Based Bowel Preparation Evaluation System
|
||
Completed |
NCT02978664 -
The Impact of Distraction on Adenoma Detection Rate
|
N/A | |
Completed |
NCT00018551 -
Chemoprevention With Folic Acid
|
Phase 2 | |
Recruiting |
NCT05594576 -
Comparison of the ENDOCUFF VISION® Endoscopy Cap Coupled With GI GENIUS™ Artificial Intelligence Compared to Each Device Alone in Improving Colonic Adenoma Detection Rate During Colonoscopy
|
N/A | |
Not yet recruiting |
NCT04135716 -
A Multicenter Study Evaluating the Effectiveness of Endo.Angel in Improving the Quality of Colonoscopy
|
N/A | |
Recruiting |
NCT02552017 -
Accuracy of Detection Using ENdocuff Optimisation of Mucosal Abnormalities
|
N/A | |
Recruiting |
NCT02288962 -
Dopamine Agonist Treatment of Non-functioning Pituitary Adenomas
|
Phase 3 | |
Completed |
NCT02066064 -
G-Eye Advanced Colonoscopy For Increased Polyp Detection Rate-randomized Tandem Study With Different Endoscopist
|
N/A | |
Completed |
NCT01749722 -
Safety and Efficacy of the NaviAid™ G-Eye System During Colonoscopy
|
N/A | |
Withdrawn |
NCT01546246 -
Water Method in Patients With Incomplete Colonoscopy
|
N/A | |
Completed |
NCT01485133 -
Water Method Colonoscopy in Patients With Prior Surgery
|
N/A | |
Withdrawn |
NCT01546259 -
Water Method in Low-body Mass Index (BMI) Female Patients With Unsedated Colonoscopy
|
N/A |