Pain Assessment Following Placement of a Percutaneous Radiologic Gastrostomy and Predictive Factors
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorCentre Hospitalier de Valence
About this trial
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.
Eligibility criteria
Qualifiers
Needing a radiologic gastrostomy under local anesthesia
Age ≥ 18 years old
Read, write and understand the French language
Disqualifiers
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
Trial design
Treatments tested in this trial
- Not listed
Trial groups
50 Participants
are grouped into 1 trial groupSponsors and collaborators
Source ClinicalTrials.gov