Actively Recruiting
Pain Assessment Following Placement of a Percutaneous Radiologic Gastrostomy and Predictive Factors
Led by Centre Hospitalier de Valence · Updated on 2026-03-18
50
Participants Needed
1
Research Sites
194 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Pain Assessment Following Placement of a Percutaneous Radiologic Gastrostomy and Predictive Factors
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Needing a radiologic gastrostomy under local anesthesia
- Age 65 18 years old
- Read, write and understand the French language
You will not qualify if you...
- Patient under guardianship, deprived of liberty, safeguard of justice
- Patient presenting a serious psychiatric pathology that does not allow compliance with the completion of the questionnaires (at the discretion of the investigator)
- Refusal to participate in research
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Sandrine Beauchard
Valence, France, 26400
Actively Recruiting
Research Team
M
Mathilde FINOT, MD
CONTACT
G
Guillaume BUIRET, MD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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