Evaluating pain after percutaneous radiologic gastrostomy placement

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to assess the abdominal pain experienced by patients following the placement of a percutaneous radiologic gastrostomy (PRG) over a 12-month period. It will evaluate the severity and prevalence of pain as well as identify predictive factors that may influence pain outcomes. The study will involve monitoring patients from baseline until seven days post-procedure to gather comprehensive data on their pain experiences. The findings could help improve patient management and care following PRG placement.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Needing a radiologic gastrostomy under local anesthesia
* Age ≥ 18 years old
* Read, write and understand the French language

Exclusion Criteria:

* 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

Where it's running

• Sandrine Beauchard
  Valence, France Recruiting

Study contacts

• Study coordinator: Mathilde FINOT, MD
• Email: mfinot@ch-valence.fr
• Phone: +33475818870

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.