RecruitingNot Applicable

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

France50 participantsStarted 2022-12-09

Plain-language 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.

Who can participate

Age range18 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

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

What they're measuring

abdominal pain

Timeframe: 7 days

predictive factors

Timeframe: DAY 1

Trial details

NCT IDNCT05618392

SponsorCentre Hospitalier de Valence

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2025-12-09

Contact for this trial

Mathilde FINOT, MD

+33475818870 mfinot@ch-valence.fr

View on ClinicalTrials.gov More Gastrostomy Complications trials