RecruitingNCT05618392

Pain Assessment Following Placement of a Percutaneous Radiologic Gastrostomy and Predictive Factors


Sponsor

Centre Hospitalier de Valence

Enrollment

50 participants

Start Date

Dec 9, 2022

Study Type

OBSERVATIONAL

Conditions

Summary

A 12 months mono-center, descriptive study, to evaluate pain and predictive factors Following placement of percutaneous Radiologic gastrostomy (PRG). The primary objective is to evaluate the abdominal pain associated with percutaneous radiologic gastrostomy (PRG) placement.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study measures and characterizes pain experienced by patients after having a radiologic gastrostomy tube placed — a feeding tube inserted through the abdomen using imaging guidance and local anesthesia (no general anesthesia). Researchers want to identify how much pain patients feel and what factors predict greater pain, to improve pain management for future patients. You may be eligible if: - You are 18 years or older - You need a gastrostomy tube placed by radiology under local anesthesia - You read, write, and understand French You may NOT be eligible if: - You are under legal guardianship, deprived of liberty, or under a justice safeguard measure - You have a serious psychiatric condition that prevents you from completing questionnaires - You refuse to participate Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

Interested in this trial?

Get notified about updates and connect with the research team.


Locations(1)

Sandrine Beauchard

Valence, France

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT05618392


Related Trials