Preparation Regimens to Improve Capsule Endoscopy Visualization and Diagnostic Yield (PrepRICE)
Primary Purpose
Obscure Gastrointestinal Bleeding
Status
Recruiting
Phase
Not Applicable
Locations
Portugal
Study Type
Interventional
Intervention
Moviprep
Sponsored by
About this trial
This is an interventional other trial for Obscure Gastrointestinal Bleeding focused on measuring Small bowel capsule endoscopy, Obscure gastrointestinal bleeding, Bowel preparation
Eligibility Criteria
Inclusion Criteria:
- Be 18 years old or older
- Present OGIB (either occult or overt)
- Agree with study's procedures and have signed the informed consent for the study and SBCE, prior to SBCE procedure
Exclusion Criteria:
- Patients performing capsule endoscopy in urgent setting for overt obscure GI bleeding
- Inpatients or bedridden
- History of surgery of the esophagus, stomach, small bowel, or colon
- History of abdominal or pelvic radiation therapy
- Suspected or confirmed stenosis or occlusion
- Suspected or confirmed bowel perforation
- Severe comorbidities, as defined by grade 3 "severe decompensation" in the Adult Comorbidity Evaluation-27 index (ACE-27)
- Pregnant women
- Patients using narcotics or prokinetics in the week before the SBCE
Sites / Locations
- Department of Gastroenterology, Centro Hospitalar Vila Nova de Gaia/EspinhoRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm Type
Experimental
Experimental
Experimental
Experimental
Arm Label
Protocol 1
Protocol 2
Protocol 3
Protocol 4
Arm Description
1L of Moviprep® solution the night before the procedure
1L of Moviprep® solution up to 2h before the procedure
0.5L of Moviprep® solution up to 2h before the procedure plus 0.5L of Moviprep® solution after the capsule had reached the duodenum
1L of Moviprep® solution after the capsule had reached the duodenum
Outcomes
Primary Outcome Measures
Diagnostic yield
Proportion of SBCE with positive findings. findings will be classified based on the Saurin classification; the investigators will consider a positive SBCE when lesions classified as P2 or active bleeding are detected (Saurin classification, Table 2), the remaining will be classified as negative
Adequate cleansing rate
A cutoff value of quantitative index ≥ 8 points
Secondary Outcome Measures
Proportion of SBCE with vascular lesions
Vascular lesions identified in each tertile
Proportion of SBCE with active bleeding
Active bleeding in each tertile
Diagnostic yield per tertile
Positive findings in each tertile
Transit times
Time of entry in the stomach, duodenum and cecum
Symptoms experienced during SBCE procedure
Nausea, vomit, bloating, abdominal pain
Overall patients' satisfaction with the cleansing regimen
rated on a 5-point scale: 1 - very easy, 2 - easy, 3 - intermediate, 4 - difficult, 5 - very difficult
Small bowel cleansing
Mean quantitative index of the distal third of small bowel
Full Information
NCT ID
NCT05140057
First Posted
October 5, 2021
Last Updated
November 17, 2021
Sponsor
Centro Hospitalar de Vila Nova de Gaia/Espinho, E.P.E.
1. Study Identification
Unique Protocol Identification Number
NCT05140057
Brief Title
Preparation Regimens to Improve Capsule Endoscopy Visualization and Diagnostic Yield
Acronym
PrepRICE
Official Title
Preparation Regimens to Improve Capsule Endoscopy Visualization and Diagnostic Yield: a Randomized Trial
Study Type
Interventional
2. Study Status
Record Verification Date
November 2021
Overall Recruitment Status
Recruiting
Study Start Date
December 1, 2021 (Anticipated)
Primary Completion Date
October 31, 2023 (Anticipated)
Study Completion Date
October 31, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Centro Hospitalar de Vila Nova de Gaia/Espinho, E.P.E.
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
Small bowel capsule endoscopy (SBCE) has become an important tool in clinical practice since its introduction in 2000. This non-invasive method allows the visualization of small bowel mucosa, being essential in the management of many conditions, such as suspected small bowel bleeding, inflammatory bowel diseases and intestinal polyposis syndromes. Despite recommendations concerning SBCE in different pathologies, there are still some technical concerns to be addressed. The optimal preparation for SBCE has been one of these controversial issues.
Currently, the European Society of Gastrointestinal Endoscopy (ESGE) recommends that patients ingest a purgative agent (2L of polyethylene glycol, PEG) and antifoaming agents for SBCE, because it was associated with a better visualization. However, it remains unclear which is the optimal timing for purgative use. Furthermore, the use of a booster agent after capsule ingestion is already performed in colon capsule endoscopy, but less is known about its application in SBCE. Also, it remains to be clarified whether a better visualization results in higher diagnostic yield and impacts patients' outcomes.
Therefore, the global aim of this prospective, randomized, multi-centric study is to determine the optimal timing and preparation for small-bowel capsule endoscopy (regardless of the equipment used), comparing four groups of different preparation protocols:
Protocol 1) 1L of Moviprep® solution the night before the procedure
Protocol 2) 1L of Moviprep® solution up to 2h before the procedure
Protocol 3) 0.5L of Moviprep® solution up to 2h before the procedure plus 0.5L of Moviprep® solution after the capsule had reached the duodenum (assessed with real-time viewer)
Protocol 4) 1L of Moviprep® solution after the capsule had reached the duodenum (assessed using real-time viewer)
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obscure Gastrointestinal Bleeding
Keywords
Small bowel capsule endoscopy, Obscure gastrointestinal bleeding, Bowel preparation
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
210 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Protocol 1
Arm Type
Experimental
Arm Description
1L of Moviprep® solution the night before the procedure
Arm Title
Protocol 2
Arm Type
Experimental
Arm Description
1L of Moviprep® solution up to 2h before the procedure
Arm Title
Protocol 3
Arm Type
Experimental
Arm Description
0.5L of Moviprep® solution up to 2h before the procedure plus 0.5L of Moviprep® solution after the capsule had reached the duodenum
Arm Title
Protocol 4
Arm Type
Experimental
Arm Description
1L of Moviprep® solution after the capsule had reached the duodenum
Intervention Type
Combination Product
Intervention Name(s)
Moviprep
Intervention Description
Bowel preparation for small bowel capsule endoscopy - same product for all groups, different administration timings
Primary Outcome Measure Information:
Title
Diagnostic yield
Description
Proportion of SBCE with positive findings. findings will be classified based on the Saurin classification; the investigators will consider a positive SBCE when lesions classified as P2 or active bleeding are detected (Saurin classification, Table 2), the remaining will be classified as negative
Time Frame
During the procedure
Title
Adequate cleansing rate
Description
A cutoff value of quantitative index ≥ 8 points
Time Frame
During the procedure
Secondary Outcome Measure Information:
Title
Proportion of SBCE with vascular lesions
Description
Vascular lesions identified in each tertile
Time Frame
During the procedure
Title
Proportion of SBCE with active bleeding
Description
Active bleeding in each tertile
Time Frame
During the procedure
Title
Diagnostic yield per tertile
Description
Positive findings in each tertile
Time Frame
During the procedure
Title
Transit times
Description
Time of entry in the stomach, duodenum and cecum
Time Frame
During the procedure
Title
Symptoms experienced during SBCE procedure
Description
Nausea, vomit, bloating, abdominal pain
Time Frame
During the procedure
Title
Overall patients' satisfaction with the cleansing regimen
Description
rated on a 5-point scale: 1 - very easy, 2 - easy, 3 - intermediate, 4 - difficult, 5 - very difficult
Time Frame
During the procedure
Title
Small bowel cleansing
Description
Mean quantitative index of the distal third of small bowel
Time Frame
During the procedure
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Be 18 years old or older
Present OGIB (either occult or overt)
Agree with study's procedures and have signed the informed consent for the study and SBCE, prior to SBCE procedure
Exclusion Criteria:
Patients performing capsule endoscopy in urgent setting for overt obscure GI bleeding
Inpatients or bedridden
History of surgery of the esophagus, stomach, small bowel, or colon
History of abdominal or pelvic radiation therapy
Suspected or confirmed stenosis or occlusion
Suspected or confirmed bowel perforation
Severe comorbidities, as defined by grade 3 "severe decompensation" in the Adult Comorbidity Evaluation-27 index (ACE-27)
Pregnant women
Patients using narcotics or prokinetics in the week before the SBCE
Facility Information:
Facility Name
Department of Gastroenterology, Centro Hospitalar Vila Nova de Gaia/Espinho
City
Vila Nova De Gaia
Country
Portugal
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Manuela Estevinho
Phone
+351 227865100
Email
mmestevinho@gmail.com
First Name & Middle Initial & Last Name & Degree
Rolando Pinho
First Name & Middle Initial & Last Name & Degree
Rolando Pinho
First Name & Middle Initial & Last Name & Degree
Ana Catarina Gomes
First Name & Middle Initial & Last Name & Degree
Ana Ponte
First Name & Middle Initial & Last Name & Degree
Adélia Rodrigues
First Name & Middle Initial & Last Name & Degree
Manuela Estevinho
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Preparation Regimens to Improve Capsule Endoscopy Visualization and Diagnostic Yield
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