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Effect of Low-volume (1L) vs Intermediate-volume (2L) Bowel Preparation on Cost-effectiveness and Quality of Life (RESULT)

Primary Purpose

Colorectal Cancer, Colonic Polyp

Status
Completed
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
Plenvu
Moviprep
Sponsored by
Radboud University Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Colorectal Cancer focused on measuring colonoscopy, bowel preparation, Quality of life, Costeffectiveness

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age > 18 years
  • Planned elective colonoscopy for surveillance or diagnostic indications

Exclusion Criteria:

  • Therapeutic colonoscopy (e.g. endoscopic mucosal resection (EMR)
  • History of (sub) total colectomy
  • Inflammatory bowel disease (IBD)
  • Inpatient status
  • Indication for an intensified bowel preparation regime
  • Emergency colonoscopy
  • Limited Dutch language skills
  • Dementia
  • Visual impairment
  • Commonly accepted contra-indications for non-iso osmotic bowel preparation and ascorbate:

    • Glucose-6-phosphate-dehydrogenase (G6PD) deficiency
    • (sub)ileus
    • Bowel obstruction or perforation
    • Acute abdomen
    • Gastroparesis
    • intolerance for any of the formulation ingredients
    • Severe renal insufficiency (creatinine clearance < 30mL/min)
    • Congestive heart failure (NYHA III or IV)
    • Phenylketonuria

Sites / Locations

  • Radboud university medical center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Pleinvue

Moviprep

Arm Description

a 1L poly ethylene glycol PEG solution with added ascorbate (Pleinvue, Norgine, active ingredients PEG 3350, Sodium ascorbate, Sodium sulfate, Ascorbic acid, Sodium chloride, Potassium chlorid)

a 2L PEG solution with added ascorbate (Moviprep, Norgine, active ingredients Macrogol 3350, Sodium Sulphate Anhydrous, Sodium chloride, Potassium chloride, Ascorbic acid, Sodium ascorbate)

Outcomes

Primary Outcome Measures

Boston Bowel preparation scale score (total and per segment)
Level of bowel cleanliness achieved with the bowel preparation used. Segmental scores range from 0 to 3, in which 0 is worst and 3 is best. A segmental score of 2 or more is considered adequate for colonoscopy.
Proportion of adequately prepared patients per type of bowel preparation
Level of bowel cleanliness achieved with the bowel preparation used. Segmental boston bowel preparation scores range from 0 to 3, in which 0 is worst and 3 is best. A segmental score of 2 or more is considered adequate for colonoscopy.

Secondary Outcome Measures

absolute score of SF-36 (short-form 36)
Change in scoring on the short-form 36 questionnaire before and after bowel preparation. Higher scores indicate a higher quality of life.
absolute score EQ-5D-5L
Change in scoring on EuroQol group 5Dimension-5Levels questionnaire before and after bowel preparation. Higher scores indicate a higher quality of life.
Correlation of clinical parameters and tolerability to Quality of life scores
Correlation of answers to questionaire on tolerability and relation to bowel cleanliness to scoring on SF-36 (short form 36) and EQ-5D-5L (EuroQol group 5 dimensions 5 levels), higher scores indicate a higher quality of life.
Subgroup differences for absolute scores on SF-36 for colonoscopy indication and prior experience with bowel preparation
Change in QoL scores on SF-36 based on having prior experience with bowel preparation, and differences between colonoscopy indications. SF-36 (short form 36), higher scores indicate a higher quality of life.
Subgroup differences in costs for colonoscopy indication and prior experience with bowel preparation
Change in costs based on having prior experience with bowel preparation, and differences between colonoscopy indications.
Subgroup differences for absolute scores on EQ-5D-5L for colonoscopy indication and prior experience with bowel preparation
Change QoL scores on EQ-5D-5L based on having prior experience with bowel preparation, and differences between colonoscopy indications. EQ-5D-5L (EuroQol group 5 dimensions 5 levels), higher scores indicate a higher quality of life.
Total individual costs
Total costs made per individual for the bowel preparation process, including cost for being absent at work and caregiver costs.
Incremental cost-effectiveness ratio
Change in costs per quality adjusted life years between the low-volume arm and intermediate volume arm.
treating physician advised surveillance interval per study arm
advised surveillance interval correlated to colonoscopy findings and BBPS (boston bowel preparation scale) score by the treating physician. Higher scores indicate higher bowel cleanliness

Full Information

First Posted
September 30, 2021
Last Updated
June 28, 2023
Sponsor
Radboud University Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT05242562
Brief Title
Effect of Low-volume (1L) vs Intermediate-volume (2L) Bowel Preparation on Cost-effectiveness and Quality of Life
Acronym
RESULT
Official Title
Effect of Low-volume (1L) vs Intermediate-volume (2L) Bowel Preparation on Cost-effectiveness and Quality of Life (RESULT Study). A Multicenter Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
August 2022
Overall Recruitment Status
Completed
Study Start Date
May 16, 2022 (Actual)
Primary Completion Date
February 28, 2023 (Actual)
Study Completion Date
March 1, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Radboud University Medical Center

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Adequate bowel preparation for colonoscopy is paramount for optimal diagnostic accuracy and safety. However, the need for high volumes to clean the colon often makes it difficult for patients to adhere to. Therefore, new low volume bowel preparation fluids have been developed. Little is known on the impact of these low volume bowel preparation fluids (1L), compared to intermediate-volume (2L) laxatives on quality of life (QoL) and cost-effectiveness. This study aims to provide further evidence on the presumed positive effect of ultra-low volume bowel preparation on patients' QoL and cost-effectiveness, in addition to its already demonstrated positive effect on bowel cleansing for colonoscopy. This multicenter randomized controlled trial (RCT) will be conducted in four hospitals in the Netherlands. Secure web-based questionnaires will be used before starting bowel preparation (baseline, t=0) and within 1 week (t=1) after colonoscopy, to assess the impact of bowel preparation on QoL and explore costs and productivity loss for cost-effectiveness analysis.
Detailed Description
Background and aims: Adequate bowel preparation for colonoscopy is paramount for optimal diagnostic accuracy and safety. However, the need for high volumes to clean the colon often makes it difficult for patients to adhere to. Therefore, new low volume bowel preparation fluids have been developed. Little is known on the impact of these low volume bowel preparation fluids (1L), compared to intermediate-volume (2L) laxatives on quality of life (QoL) and cost-effectiveness. This study aims to provide further evidence on the presumed positive effect of ultra-low volume bowel preparation on patients' QoL and cost-effectiveness, in addition to its already demonstrated positive effect on bowel cleansing for colonoscopy. Study design: This multicenter randomized controlled trial (RCT) will be conducted in four hospitals in the Netherlands. Secure web-based questionnaires will be used before starting bowel preparation (baseline, t=0) and within 1 week (t=1) after colonoscopy, to assess the impact of bowel preparation on QoL and explore costs and productivity loss for cost-effectiveness analysis. Data on colonoscopy findings and complications will be retrieved from the patients' medical record. Study population: This multicenter study will include 470 patients from 4 hospitals. Intervention: Patients will be randomized during the pre-colonoscopy hospital visit between a specialized low-volume 1-liter bowel preparation fluid (Pleinvue) or an intermediate-volume 2-liter bowel preparation fluid (Moviprep), which are already both routinely used as bowel preparation for colonoscopy in the Netherlands. Nature and extent of the burden and risks associated with participation, benefit and group relatedness: There is no direct benefit for patients participating in this study. Risk associated with participation are considered minimal, and are limited to the possibility of privacy related issues. Nonetheless, this is considered to be minimal because of the use of pseudonymized data and GDPR compliant databases. In the future, results from this study could possibly benefit patients undergoing colonoscopy, with the possibility of reducing the need for repeat colonoscopies and improving patient experience of colonoscopies.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colorectal Cancer, Colonic Polyp
Keywords
colonoscopy, bowel preparation, Quality of life, Costeffectiveness

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Patients will be randomized during the pre-colonoscopy hospital visit between a specialized low-volume 1-liter bowel preparation fluid (Pleinvue) or an intermediate-volume 2-liter bowel preparation fluid (Moviprep)
Masking
None (Open Label)
Allocation
Randomized
Enrollment
509 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Pleinvue
Arm Type
Experimental
Arm Description
a 1L poly ethylene glycol PEG solution with added ascorbate (Pleinvue, Norgine, active ingredients PEG 3350, Sodium ascorbate, Sodium sulfate, Ascorbic acid, Sodium chloride, Potassium chlorid)
Arm Title
Moviprep
Arm Type
Active Comparator
Arm Description
a 2L PEG solution with added ascorbate (Moviprep, Norgine, active ingredients Macrogol 3350, Sodium Sulphate Anhydrous, Sodium chloride, Potassium chloride, Ascorbic acid, Sodium ascorbate)
Intervention Type
Drug
Intervention Name(s)
Plenvu
Other Intervention Name(s)
Pleinvue
Intervention Description
a recently developed 1 liter bowel preparation fluid that is often used in clinical practice. Patients will receive a split dose protocol, low-residue diet 2 days before colonoscopy, and clear liquid diet 1 day before colonoscopy.
Intervention Type
Drug
Intervention Name(s)
Moviprep
Intervention Description
a 2 liter widely established 2 liter bowel preparation fluid that is commonly used in clinical practice. Patients will receive a split dose protocol, low-residue diet 2 days before colonoscopy, and clear liquid diet 1 day before colonoscopy.
Primary Outcome Measure Information:
Title
Boston Bowel preparation scale score (total and per segment)
Description
Level of bowel cleanliness achieved with the bowel preparation used. Segmental scores range from 0 to 3, in which 0 is worst and 3 is best. A segmental score of 2 or more is considered adequate for colonoscopy.
Time Frame
during colonoscopy procedure
Title
Proportion of adequately prepared patients per type of bowel preparation
Description
Level of bowel cleanliness achieved with the bowel preparation used. Segmental boston bowel preparation scores range from 0 to 3, in which 0 is worst and 3 is best. A segmental score of 2 or more is considered adequate for colonoscopy.
Time Frame
during colonoscopy procedure
Secondary Outcome Measure Information:
Title
absolute score of SF-36 (short-form 36)
Description
Change in scoring on the short-form 36 questionnaire before and after bowel preparation. Higher scores indicate a higher quality of life.
Time Frame
within 1 week after colonoscopy, questionnaire 2/2
Title
absolute score EQ-5D-5L
Description
Change in scoring on EuroQol group 5Dimension-5Levels questionnaire before and after bowel preparation. Higher scores indicate a higher quality of life.
Time Frame
within 1 week after colonoscopy, questionnaire 2/2
Title
Correlation of clinical parameters and tolerability to Quality of life scores
Description
Correlation of answers to questionaire on tolerability and relation to bowel cleanliness to scoring on SF-36 (short form 36) and EQ-5D-5L (EuroQol group 5 dimensions 5 levels), higher scores indicate a higher quality of life.
Time Frame
questionnaire 2/2, within 1 week after colonoscopy
Title
Subgroup differences for absolute scores on SF-36 for colonoscopy indication and prior experience with bowel preparation
Description
Change in QoL scores on SF-36 based on having prior experience with bowel preparation, and differences between colonoscopy indications. SF-36 (short form 36), higher scores indicate a higher quality of life.
Time Frame
questionnaire 2/2, within 1 week after colonoscopy
Title
Subgroup differences in costs for colonoscopy indication and prior experience with bowel preparation
Description
Change in costs based on having prior experience with bowel preparation, and differences between colonoscopy indications.
Time Frame
questionnaire 2/2, within 1 week after colonoscopy
Title
Subgroup differences for absolute scores on EQ-5D-5L for colonoscopy indication and prior experience with bowel preparation
Description
Change QoL scores on EQ-5D-5L based on having prior experience with bowel preparation, and differences between colonoscopy indications. EQ-5D-5L (EuroQol group 5 dimensions 5 levels), higher scores indicate a higher quality of life.
Time Frame
questionnaire 2/2, within 1 week after colonoscopy
Title
Total individual costs
Description
Total costs made per individual for the bowel preparation process, including cost for being absent at work and caregiver costs.
Time Frame
questionnaire 2/2, within 1 week after colonoscopy
Title
Incremental cost-effectiveness ratio
Description
Change in costs per quality adjusted life years between the low-volume arm and intermediate volume arm.
Time Frame
within 1 week after colonoscopy, questionnaire 2/2
Title
treating physician advised surveillance interval per study arm
Description
advised surveillance interval correlated to colonoscopy findings and BBPS (boston bowel preparation scale) score by the treating physician. Higher scores indicate higher bowel cleanliness
Time Frame
During colonoscopy procedure

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age > 18 years Planned elective colonoscopy for surveillance or diagnostic indications Exclusion Criteria: Therapeutic colonoscopy (e.g. endoscopic mucosal resection (EMR) History of (sub) total colectomy Inflammatory bowel disease (IBD) Inpatient status Indication for an intensified bowel preparation regime Emergency colonoscopy Limited Dutch language skills Dementia Visual impairment Commonly accepted contra-indications for non-iso osmotic bowel preparation and ascorbate: Glucose-6-phosphate-dehydrogenase (G6PD) deficiency (sub)ileus Bowel obstruction or perforation Acute abdomen Gastroparesis intolerance for any of the formulation ingredients Severe renal insufficiency (creatinine clearance < 30mL/min) Congestive heart failure (NYHA III or IV) Phenylketonuria
Facility Information:
Facility Name
Radboud university medical center
City
Nijmegen
State/Province
Gelderland
ZIP/Postal Code
6525GA
Country
Netherlands

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
The dataset used during this study is available from the corresponding author upon reasonable request
IPD Sharing Time Frame
15y
IPD Sharing Access Criteria
The dataset used during this study is available from the corresponding author upon reasonable request

Learn more about this trial

Effect of Low-volume (1L) vs Intermediate-volume (2L) Bowel Preparation on Cost-effectiveness and Quality of Life

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