search
Back to results

Exploratory Investigation on a Novel Catheter

Primary Purpose

Bowel Dysfunction

Status
Recruiting
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
Transanal irrigation (TAI)
Sponsored by
Wellspect HealthCare
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Bowel Dysfunction

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Provision of informed consent. Female and male aged 18-80 years. Patients successfully treated by TAI with Navina Smart system for at least 3 months and/or stable in therapy. Patients considered suitable to participate by investigator. Able to read, write and understand information given to them regarding the study. Exclusion Criteria: Involvement in the planning and conduct of the clinical investigation (applies to both Wellspect HealthCare staff and staff at the study site). Previous enrolment in the present clinical investigation. Simultaneous participation in another clinical investigation, or participation in a clinical investigation during the last month, that may interfere with the present clinical investigation. Severe non-compliance to Clinical Investigation Plan as judged by the investigator and/or Wellspect HealthCare. Significant cardiovascular and/or other significant co-morbidities which could be negatively affected by the use of the investigational product. Known anal or colorectal stenosis. Active inflammatory bowel disease. Acute diverticulitis. Colorectal cancer. Ischemic colitis. Any anal or colorectal surgery within the previous 3 months. Anal, rectal and/or colonic endoscopic polypectomy within the previous 4 weeks. Any condition, as judged by the investigator, which might make follow-up or investigations inappropriate. Any patient that according to the Declaration of Helsinki is unsuitable for enrolment.

Sites / Locations

  • Proctos KliniekRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

All subjects

Arm Description

Transanal irrigation (TAI) with new catheter

Outcomes

Primary Outcome Measures

Catheter stay in place
Does the catheter stay in place during water instillation? Yes/No

Secondary Outcome Measures

Bowel emptying performance
Evaluation of bowel emptying performance: Subject's perception of emptying of bowel similar to regular use of TAI. Descriptive analysis of data from questionnaires at Visit 2 and 3 collected from subject's previous experience from using balloon catheter comparing it with experience of using two different sizes of study catheters during study. Question asked: "What is the subject's perception of emptying of bowel with the study catheter compared to their regular use with a balloon catheter?" Potential response: much worse, worse, same, better, much better
Leakage
Evaluation of leakage during water instillation: Subject's perception of leakage similar to regular use of TAI. Descriptive analysis of data from questionnaires at Visit 2 and 3 collected from subject's previous experience from using balloon catheter comparing it with experience of using two different sizes of study catheters during study. Question asked: "What is the subject's perception of leakage with the study catheter compared to their regular use with a balloon catheter?" Potential response: much worse, worse, same, better, much better

Full Information

First Posted
November 18, 2022
Last Updated
April 25, 2023
Sponsor
Wellspect HealthCare
search

1. Study Identification

Unique Protocol Identification Number
NCT05644912
Brief Title
Exploratory Investigation on a Novel Catheter
Official Title
Exploratory Investigation on a Novel Catheter
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Recruiting
Study Start Date
November 18, 2022 (Actual)
Primary Completion Date
September 30, 2023 (Anticipated)
Study Completion Date
September 30, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Wellspect HealthCare

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
An exploratory, pre-market, open, prospective, interventional, clinical investigation at a limited number of centers for proof of concept of a new catheter. In this proof of concept investigation, subjects experienced in using transanal irrigation (TAI) with a balloon catheter will be using study catheters at two occasions to primarily study if the catheter will stay in place during the water instillation when performing TAI. Each subject will be followed during approximately one week, depending on the usual time between their TAI.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bowel Dysfunction

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Proof of concept investigation with subjects experienced in using transanal irrigation with a balloon catheter.
Masking
None (Open Label)
Allocation
N/A
Enrollment
15 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
All subjects
Arm Type
Experimental
Arm Description
Transanal irrigation (TAI) with new catheter
Intervention Type
Device
Intervention Name(s)
Transanal irrigation (TAI)
Intervention Description
Transanal irrigation (TAI) with new catheter on subjects experienced in using TAI with balloon catheter.
Primary Outcome Measure Information:
Title
Catheter stay in place
Description
Does the catheter stay in place during water instillation? Yes/No
Time Frame
1 week
Secondary Outcome Measure Information:
Title
Bowel emptying performance
Description
Evaluation of bowel emptying performance: Subject's perception of emptying of bowel similar to regular use of TAI. Descriptive analysis of data from questionnaires at Visit 2 and 3 collected from subject's previous experience from using balloon catheter comparing it with experience of using two different sizes of study catheters during study. Question asked: "What is the subject's perception of emptying of bowel with the study catheter compared to their regular use with a balloon catheter?" Potential response: much worse, worse, same, better, much better
Time Frame
1 week
Title
Leakage
Description
Evaluation of leakage during water instillation: Subject's perception of leakage similar to regular use of TAI. Descriptive analysis of data from questionnaires at Visit 2 and 3 collected from subject's previous experience from using balloon catheter comparing it with experience of using two different sizes of study catheters during study. Question asked: "What is the subject's perception of leakage with the study catheter compared to their regular use with a balloon catheter?" Potential response: much worse, worse, same, better, much better
Time Frame
1 week
Other Pre-specified Outcome Measures:
Title
Safety: Adverse Events and Device Deficiencies
Description
To evaluate the safety of catheter by assessment of incidence and severity of Adverse Events (AEs, SAEs, ADEs, SADEs, USADEs) and Device Deficiencies occurring during the study period.
Time Frame
1 week

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Provision of informed consent. Female and male aged 18-80 years. Patients successfully treated by TAI with Navina Smart system for at least 3 months and/or stable in therapy. Patients considered suitable to participate by investigator. Able to read, write and understand information given to them regarding the study. Exclusion Criteria: Involvement in the planning and conduct of the clinical investigation (applies to both Wellspect HealthCare staff and staff at the study site). Previous enrolment in the present clinical investigation. Simultaneous participation in another clinical investigation, or participation in a clinical investigation during the last month, that may interfere with the present clinical investigation. Severe non-compliance to Clinical Investigation Plan as judged by the investigator and/or Wellspect HealthCare. Significant cardiovascular and/or other significant co-morbidities which could be negatively affected by the use of the investigational product. Known anal or colorectal stenosis. Active inflammatory bowel disease. Acute diverticulitis. Colorectal cancer. Ischemic colitis. Any anal or colorectal surgery within the previous 3 months. Anal, rectal and/or colonic endoscopic polypectomy within the previous 4 weeks. Any condition, as judged by the investigator, which might make follow-up or investigations inappropriate. Any patient that according to the Declaration of Helsinki is unsuitable for enrolment.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Peter Taffo
Phone
+46313764000
Ext
3390
Email
peter.taffo@wellspect.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ingrid Han-Geurts, MD
Organizational Affiliation
Proctos Kliniek
Official's Role
Principal Investigator
Facility Information:
Facility Name
Proctos Kliniek
City
Bilthoven
State/Province
MB Bilthoven
ZIP/Postal Code
3723
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ingrid Han-Geurts, MD
Phone
+31 30 225 02 60
Email
info@proctoskliniek.nl

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
IPD available will not be available to other researchers.

Learn more about this trial

Exploratory Investigation on a Novel Catheter

We'll reach out to this number within 24 hrs