Clinical Trials Directory

Trials / Recruiting

RecruitingNCT05618392

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

Status
Recruiting
Phase
Study type
Observational
Enrollment
50 (estimated)
Sponsor
Centre Hospitalier de Valence · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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.

Detailed 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

Conditions

Timeline

Start date
2022-12-09
Primary completion
2025-12-09
Completion
2026-09-01
First posted
2022-11-16
Last updated
2026-03-18

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT05618392. Inclusion in this directory is not an endorsement.