Feasibility of a Constant Pressure Skin Disk (CPSD) in Enteral Tubes

Overview

About this study

The purpose of this research study is to gather information on one specific part of a feeding tube, known as the adjustable skin disk. The goal of this research study is to see if a new type of adjustable skin disk, called a Constant Pressure Skin Disk (CPSD), can safely and effectively support one or more of the following: 1) adequate healing after feeding tube placement; 2) a reduced rate of complications associated with feeding tubes, such as leakage, skin breakdown, etc.; 3) ease of use; and 4) durability (holds up to usual wear and tear associated with feeding tube use).

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  • Non-hospitalized outpatients who are undergoing initial placement of an enteral gastrostomy (G) or jejunostomy (J) tube.  
  • Age ≥ 22 years.

Exclusion Criteria: 

  • Current or history of illegal drug use in the past year.
  • Current tobacco use.
  • History of a percutaneous enteral tube.
  • History of gastric surgery (bariatric surgery, Nissen fundoplication, etc.).

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Rochester, Minn.

Mayo Clinic principal investigator

Manpreet Mundi, M.D.

Open for enrollment

Contact information:

Manpreet Mundi M.D.

(507) 284-4080

Mundi.Manpreet@mayo.edu

More information

Publications

Publications are currently not available