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

Gastrostomy Clinical Trial

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

Clinical Trial 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.

Clinical Trial Description

PRG is a pathway first of all enteral nutrition that has several advantages: local anesthesia, possible in case of esophageal stenosis, Rates of successful tube placement higher for radiologic gastrostomy than for percutaneous endoscopic Gastrostomy (PEG). Abdominal pain following percutaneous radiologic gastrostomy (PRG) placement is a recognized complication. However, the prevalence and degree of severity of pain are poorly characterized. This pain often requires antalgic treatment. The primary objective is to evaluate the abdominal pain from Baseline until 7 days after radiologic gastrostomy (PRG) placement. The secondary objective is to evaluate predictive factors ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05618392
Study type Observational
Source Centre Hospitalier de Valence
Contact Mathilde FINOT, MD
Phone +33475818870
Email mfinot@ch-valence.fr
Status Recruiting
Phase
Start date December 9, 2022
Completion date January 1, 2026
View Details
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