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Mic-Key Versus Mini One Family Preference Comparison (MicKeyVMini)

Primary Purpose

Gastroesophageal Reflux, Feeding Disorder, Family Satisfaction

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
GT button change - Mic-Key
GT button change - Mini One
Sponsored by
Children's Mercy Hospital Kansas City
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Gastroesophageal Reflux focused on measuring Gastroesophageal Reflux, Feeding Disorder, Gastrostomy tube, Family Satisfaction, GT button, Enteral nutrition, Gastrostomy button

Eligibility Criteria

1 Day - 5 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Children ages 0-5 years of age requiring 0.8 cm or 1.0 cm gastrostomy feeding devices for enteral nutrition seen in the Surgery, GI or Special Care clinics
  • Gastrostomy placement after IRB approval (enrollment will continue until 170 evaluable subjects have completed the 4 month visit. Expected attrition for the 4 year follow-up is 40%.
  • English-speaking families

Exclusion Criteria:

  • Children with dermatologic conditions influencing gastrostomy site healing and tract epithelialization
  • Children with immunosuppression
  • Children with active malignancy requiring treatment
  • Inability to commit to 4 months follow up

Sites / Locations

  • Children's Mercy Kansas City

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

GT button change - Mic-Key

GT button change - Mini One

Arm Description

Subjects randomized to the Mic-Key arm will have the Mic-Key button placed initially at surgery, and at the first gastrostomy change in the clinic at 2 months, will change to the Mini One button. At the routine 4-month visit, parents will be asked which button they prefer to keep.

Subjects randomized to the Mini One arm will have the Mini One button placed initially at surgery, and at the first gastrostomy change in the clinic at 2 months, will change to the Mic-Key button. At the routine 4-month visit, parents will be asked which button they prefer to keep.

Outcomes

Primary Outcome Measures

Parent preference
Parents will be asked which button they prefer to keep at the 4-month visit.

Secondary Outcome Measures

Enteral Access Assessment Sheet
Providers will complete a brief checklist of gastrostomy tube maintenance and site complications at the 2-month button change, 4-month visit, and all subsequent follow-up visits while the button while the G-tube remains in place.

Full Information

First Posted
January 9, 2017
Last Updated
October 19, 2021
Sponsor
Children's Mercy Hospital Kansas City
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1. Study Identification

Unique Protocol Identification Number
NCT03041649
Brief Title
Mic-Key Versus Mini One Family Preference Comparison
Acronym
MicKeyVMini
Official Title
Mic-Key Versus Mini: A Prospective, Randomized Trial for Family Preference Comparing Low Profile Balloon Gastrostomy Buttons
Study Type
Interventional

2. Study Status

Record Verification Date
October 2021
Overall Recruitment Status
Completed
Study Start Date
November 2016 (undefined)
Primary Completion Date
April 2020 (Actual)
Study Completion Date
April 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Children's Mercy Hospital Kansas City

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The objective of this study is to compare two low profile balloon gastrostomy button enteral feeding devices, both currently used as standard of medical care. The investigators aim to compare family preference and rate of complications between the two devices in a prospective cohort of children. This is the first step in comparing initial and long-term outcomes along with the need for seeking medical advice for gastrostomy site-related complications. The secondary aim of this study is to follow this population long term (4 years) to document the prevalence of: granulation tissue, infection, skin breakdown, and how long the gastrostomy tube balloon remains functional (does not lose water).
Detailed Description
This is a single center prospective, randomized study with a crossover design, comparing two low profile balloon gastrostomy buttons (Figure 1), MIC-Key™ and MINI One™ that are routinely used at CMH. Each subject will be randomly assigned to one button type at the time of initial placement. After placement, standard practice is to perform the first gastrostomy change in the clinic at 2 months where the primary caregivers replace the button under supervision. Therefore, the initial device after randomization will remain in place for 2 months. At the first scheduled device change, the other type of button will replace the original gastrostomy button device. This will remain in place for another 2 months. At the routine visit at 4 months the parents will be asked to choose which button they prefer to keep. This will meet the primary outcome endpoint of the study. The investigators will continue to follow as many subjects as possible to 4 years in order to identify any potential differences in secondary end points. A caregiver satisfaction survey is routinely used in the clinics. Parent responses to this survey will be also be used in the study analysis.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gastroesophageal Reflux, Feeding Disorder, Family Satisfaction
Keywords
Gastroesophageal Reflux, Feeding Disorder, Gastrostomy tube, Family Satisfaction, GT button, Enteral nutrition, Gastrostomy button

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
158 (Actual)

8. Arms, Groups, and Interventions

Arm Title
GT button change - Mic-Key
Arm Type
Active Comparator
Arm Description
Subjects randomized to the Mic-Key arm will have the Mic-Key button placed initially at surgery, and at the first gastrostomy change in the clinic at 2 months, will change to the Mini One button. At the routine 4-month visit, parents will be asked which button they prefer to keep.
Arm Title
GT button change - Mini One
Arm Type
Active Comparator
Arm Description
Subjects randomized to the Mini One arm will have the Mini One button placed initially at surgery, and at the first gastrostomy change in the clinic at 2 months, will change to the Mic-Key button. At the routine 4-month visit, parents will be asked which button they prefer to keep.
Intervention Type
Other
Intervention Name(s)
GT button change - Mic-Key
Intervention Description
After 2 months with each button, parents will be asked which button they prefer at the 4-month post-operational follow-up visit.
Intervention Type
Other
Intervention Name(s)
GT button change - Mini One
Intervention Description
After 2 months with each button, parents will be asked which button they prefer at the 4-month post-operational follow-up visit.
Primary Outcome Measure Information:
Title
Parent preference
Description
Parents will be asked which button they prefer to keep at the 4-month visit.
Time Frame
4 months
Secondary Outcome Measure Information:
Title
Enteral Access Assessment Sheet
Description
Providers will complete a brief checklist of gastrostomy tube maintenance and site complications at the 2-month button change, 4-month visit, and all subsequent follow-up visits while the button while the G-tube remains in place.
Time Frame
Up to 4 years after button placement

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Day
Maximum Age & Unit of Time
5 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Children ages 0-5 years of age requiring 0.8 cm or 1.0 cm gastrostomy feeding devices for enteral nutrition seen in the Surgery, GI or Special Care clinics Gastrostomy placement after IRB approval (enrollment will continue until 170 evaluable subjects have completed the 4 month visit. Expected attrition for the 4 year follow-up is 40%. English-speaking families Exclusion Criteria: Children with dermatologic conditions influencing gastrostomy site healing and tract epithelialization Children with immunosuppression Children with active malignancy requiring treatment Inability to commit to 4 months follow up
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Shawn D St. Peter, MD
Organizational Affiliation
Children's Mercy Hospital Kansas City
Official's Role
Principal Investigator
Facility Information:
Facility Name
Children's Mercy Kansas City
City
Kansas City
State/Province
Missouri
ZIP/Postal Code
64108
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
31834114
Citation
Abdelhadi RA, Dekonenko C, Dorman RM, Oyetunji TA, St Peter SD. A Prospective, Randomized Cross-over Trial of 2 Low-profile Gastrostomy Buttons to Determine Family Preference. J Pediatr Gastroenterol Nutr. 2020 Mar;70(3):386-388. doi: 10.1097/MPG.0000000000002585.
Results Reference
derived

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Mic-Key Versus Mini One Family Preference Comparison

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