NCT05618392 Pain Assessment Following Placement of a Percutaneous Radiologic Gastrostomy and Predictive Factors
| NCT ID | NCT05618392 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Centre Hospitalier de Valence |
| Condition | Gastrostomy Complications |
| Study Type | OBSERVATIONAL |
| Enrollment | 50 participants |
| Start Date | 2022-12-09 |
| Primary Completion | 2025-12-09 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.
This trial targets 50 participants in total. It began in 2022-12-09 with a primary completion date of 2025-12-09.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief 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.
Eligibility Criteria
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
Contact & Investigator
Frequently Asked Questions
Who can join the NCT05618392 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, studying Gastrostomy Complications. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT05618392 currently recruiting?
Yes, NCT05618392 is actively recruiting participants. Contact the research team at mfinot@ch-valence.fr for enrollment information.
Where is the NCT05618392 trial being conducted?
This trial is being conducted at Valence, France.
Who is sponsoring the NCT05618392 clinical trial?
NCT05618392 is sponsored by Centre Hospitalier de Valence. The trial plans to enroll 50 participants.