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

NCT05618392 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 50

Last updated 2026-03-18

No results posted yet for this study

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.

Conditions

  • Gastrostomy Complications
  • Gastrostomy

Sponsors & Collaborators

  • Centre Hospitalier de Valence

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-12-09
Primary Completion
2025-12-09
Completion
2026-09-01

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05618392 on ClinicalTrials.gov