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G-tech WPS for Bowel Function

N/A
Waitlist Available
Research Sponsored by Yale University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Eighteen (18) years of age or older
Subject has undergone or will undergo a laparoscopic or open colorectal surgery with resection and anastomosis
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 30 days after index surgery
Awards & highlights

Study Summary

This trial is to study if a wireless patch system can help predict when a post-operative patient is ready for discharge.

Who is the study for?
This trial is for adults who've had or will have colorectal surgery with resection and anastomosis, can follow the study's requirements, and consent to participate. It excludes pregnant individuals or those with allergies to medical grade adhesives.Check my eligibility
What is being tested?
The G-Tech Wireless Patch System (WPS) is being tested to see if it can predict recovery times after abdominal surgery by measuring myoelectrical activity. This could help decide when patients should start eating again and possibly when they're ready to go home.See study design
What are the potential side effects?
There are no direct side effects mentioned for using the G-Tech WPS as it's a noninvasive monitoring device. However, there may be discomfort or skin irritation due to the adhesive used in the patch system.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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I am 18 years old or older.
Select...
I have had or will have surgery to remove part of my colon and reattach the ends.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~30 days after index surgery
This trial's timeline: 3 weeks for screening, Varies for treatment, and 30 days after index surgery for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
GI Functional Recovery
Secondary outcome measures
Postoperative Ileus
Readmission with ileus

Trial Design

1Treatment groups
Experimental Treatment
Group I: Postoperative recovery with G-tech WPSExperimental Treatment1 Intervention

Find a Location

Who is running the clinical trial?

Yale UniversityLead Sponsor
1,837 Previous Clinical Trials
2,728,213 Total Patients Enrolled
G-Tech CorporationIndustry Sponsor
4 Previous Clinical Trials
524 Total Patients Enrolled

Media Library

G-tech WPS (Other) Clinical Trial Eligibility Overview. Trial Name: NCT05298774 — N/A
Paralytic Ileus Research Study Groups: Postoperative recovery with G-tech WPS
Paralytic Ileus Clinical Trial 2023: G-tech WPS Highlights & Side Effects. Trial Name: NCT05298774 — N/A
G-tech WPS (Other) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05298774 — N/A

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Is this research endeavor accessible to individuals seeking treatment?

"Unfortunately, clinicaltrials.gov reports that this particular study is not currently open to recruitment. It was initially posted on June 1st 2022 and last updated on the 9th of June 2022; however, there are 80 other medical studies actively accepting patients at the moment."

Answered by AI
~37 spots leftby Sep 2024