Bowel Cleansing Performance of the Pure-Vu System in Patients With a History of Poor Bowel Preparation

Colorectal Cancer Clinical Trial

Official title:

A New Method for Bowel Cleansing in Patients With a History of Poor Bowel Preparation - A Multicenter Feasibility Study With the Pure-Vu System

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04700410
• Other study ID #: NL66613.091.18
• Status: Completed
• Phase: N/A
• Start date: June 1, 2021
• Est. completion date: May 1, 2022

Study information

• Verified date: August 2022
• Source: Radboud University Medical Center
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The diagnostic accuracy and safety of colonoscopy highly depends on the quality of the pre-procedural bowel preparation. A past history of poor bowel preparation is the most important risk factor of inadequate bowel cleansing at the next colonoscopy. This study aims to evaluate if an adequate level of bowel cleansing can be achieved with the Pure-Vu System in patients with previous poor bowel preparation, in a single arm international multicenter feasibility study.

Description:

Rationale: It is widely acknowledged that the efficacy and safety of colonoscopy depends on the quality of the pre-procedural bowel preparation. Despite its importance, the proportion of colonoscopies with inadequate bowel preparation still ranges from 6.8-33% across studies. A past history of poor bowel preparation is the most important risk factor of inadequate bowel cleansing at the next colonoscopy. (1, 2) Evidence to recommend a specific bowel cleansing regimen in these patients is currently lacking. (3) Mostly, patients with previous bowel preparation are advised to drink more oral purgatives, which is very difficult and unpleasant for patients and therefore often fails. The aim of this study is to evaluate if an intra-procedural bowel cleaning device, the Pure-VuTM System (Tirat Carmel, Israel) can be used to achieve an adequate level of bowel cleansing in patients with previous poor bowel preparation. Objective: The aim of this study is to evaluate if an adequate level of bowel cleansing can be achieved with the Pure-Vu System in patients with previous poor bowel preparation (Boston Bowel Preparation Scale [BBPS]<6). Study design: We will perform a single arm international multicenter colonoscopy trial. Adult patients with previous poor bowel preparation (BBPS<6) will be invited to participate in our study (n= 44). All patients willing to participate will receive a limited bowel preparation (2-days of dietary restrictions + 2x 150ml picoprep) followed by intra-procedural bowel cleansing with the Pure-Vu System. The BBPS will be assessed before and after segmental washing by the endoscopist who performs the procedure and later by an independent endoscopist (photos). Study population: Adult patients with poor bowel preparation within the last 2 years. Exclusion criteria; previous colon resection, previous colorectal cancer, colitis, lower gastrointestinal bleeding with hemodynamic instability, ASA>3, insufficiently corrected anticoagulation disorders, inability to provide informed consent. Primary endpoint: The primary endpoint of the study will be the BBPS-score before and after intra-procedural bowel cleaning with the Pure-Vu System. Secondary endpoints include: - Total number of colon lesions specified by histology - Adenoma detection rate - Cecal intubation rates - Procedure times (total procedure time, cecal intubation time, withdrawal time, time for all other interventions) - Total amount of water used for washing and total amount of fluids+residual stool removed. - Patient reported outcomes (level of discomfort during bowel preparation and during colonoscopy on a visual analog scale) - System usability - Endoscopists' learning curve - Safety outcomes Nature and extent of the burden and risk associated with participation, benefit and group relatedness: Colonoscopy is a commonly performed procedure and the overall serious adverse event (SAE) rate is low, around 2.8 per 1000 colonoscopies. The risk of adverse events (AE) with the Pure-Vu are believed to be equivalent to conventional colonoscopy, including bleeding and perforation risks (13). Participation in this study could potentially benefit colonoscopy patients because the Pure-Vu is expected to improve the quality of colonoscopy. Inadequate bowel cleansing may be prevented by the Pure-Vu System. Inadequate bowel cleansing is associated with lower adenoma detection rates (ADR), lower completion rates, longer procedure times, more complications and a higher need for repeat procedures.(4, 5) In addition, Pure-Vu reduces the reliance on patients pre-procedural bowel preparation which is often considered the most deterrent part of colonoscopy by patients.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 44
• Est. completion date: May 1, 2022
• Est. primary completion date: March 28, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 80 Years

Eligibility

Inclusion Criteria:

• Patients, aged between 18 and 80 years, referred and scheduled for either screening, diagnostic, or surveillance colonoscopy.
• Poor bowel preparation within the last 2 years, defined as a BBPS <6 or need for repeat colonoscopy or shortening of surveillance interval due to poor bowel preparation

Exclusion Criteria:

• Prior colon resection
• Previous colorectal cancer
• Colitis
• Lower gastrointestinal bleeding with hemodynamic instability
• Bowel obstruction
• Pregnancy or lactating
• ASA > 3
• Insufficiently corrected anticoagulation disorders
• Inability to provide informed consent

Related Conditions & MeSH terms

• Adenoma
• Bowel Preparation
• Colonic Adenoma
• Colorectal Cancer
• Colorectal Neoplasms

Intervention

Device:
• Pure-Vu System
All patients willing to participate will receive a limited bowel preparation (2-days of dietary restrictions + 2x 150ml picoprep) followed by intra-procedural bowel cleansing with the Pure-Vu System.

Locations

Country	Name	City	State
Germany	University Medical Center Mainz	Mainz
Netherlands	Radboud university medical center	Nijmegen	Gelderland

Sponsors (3)

Lead Sponsor	Collaborator
Radboud University Medical Center	Motus GI Medical Technologies Ltd, University Medical Center Mainz

Countries where clinical trial is conducted

Germany,  Netherlands, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Boston Bowel Preparation scale (BBPS)-score before cleaning with the Pure-Vu system.	Boston Bowel Preparation scale (BBPS): The adequacy of bowel preparation should be assessed after all appropriate efforts to clear residual debris is completed. All three bowel regions of the colon will be scored (i.e., the right colon, transverse colon, and left colon) from 0-3 points by the endoscopist. The segment scores are summed for a total BBPS ranging from 0 to 9. The points will be assigned as follows: 0) Unprepared colon segment with mucosa not seen because of solid stool that could not be cleared.; Portion of mucosa of the colon segment seen, but other areas of the colon segment are not well seen because of staining, residual stool, and/or opaque liquid.; Minor amount of residual staining, small fragments of stool, and/or opaque liquid but mucosa of colon segment seen well.; Entire mucosa of colon segment seen well, with no residual staining, small fragments of stool, or opaque liquid. Each segment of the colon received a segmental score from 0- 3.	1 day (day of intervention)
Primary	Boston Bowel Preparation scale (BBPS)-score after cleaning with the Pure-Vu system.	Boston Bowel Preparation scale (BBPS): The adequacy of bowel preparation should be assessed after all appropriate efforts to clear residual debris is completed. All three bowel regions of the colon will be scored (i.e., the right colon, transverse colon, and left colon) from 0-3 points by the endoscopist. The segment scores are summed for a total BBPS ranging from 0 to 9. The points will be assigned as follows: 0) Unprepared colon segment with mucosa not seen because of solid stool that could not be cleared.; Portion of mucosa of the colon segment seen, but other areas of the colon segment are not well seen because of staining, residual stool, and/or opaque liquid.; Minor amount of residual staining, small fragments of stool, and/or opaque liquid but mucosa of colon segment seen well.; Entire mucosa of colon segment seen well, with no residual staining, small fragments of stool, or opaque liquid. Each segment of the colon received a segmental score from 0- 3.	1 day (day of intervention)
Secondary	Total number of colon lesions specified by histology		1 day (day of intervention)
Secondary	Adenoma detection rate		1 day (day of intervention)
Secondary	Cecal intubation rates		1 day (day of intervention)
Secondary	Procedure times (total procedure time, cecal intubation time, withdrawal time, time for all other interventions)		1 day (day of intervention)
Secondary	Total amount of water used for washing and total amount of fluids+residual stool removed.		1 day (day of intervention)
Secondary	Patient reported outcomes (level of discomfort during bowel preparation and during colonoscopy on a visual analog scale)	A visual analogue scale from 0 to 10, in which higher numbers indicate a higher level of discomfort.	1 month
Secondary	System usability	general ease of use, ease of rectum insertion, ease of angulation, ease of advancement, device stiffness, ease of polyp resection holding forces, ease of retroflexion,; Unacceptable; Difficult; Acceptable; Good (as good as conventional colonoscopy); Excellent	through study completion, an average of 1 year
Secondary	Endoscopists' learning curve		through study completion, an average of 1 year
Secondary	Number of adverse events after study intervention	Safety outcomes (adverse events): Severe adverse events will be subcategorized cardiac (cardiac ischemia, heart failure, arrhythmia, other) pulmonary (exacerbation of Chronic Obstructive Pulmonary Disease, infectious, other), neurological (stroke, cerebrovascular accident, bleeding, other), and other (surgical interventions etc.).	48 hours and 1month after intervention