Actively Recruiting
Phage Safety Retrospective Cohort Study
Led by Hospices Civils de Lyon · Updated on 2023-04-13
25
Participants Needed
1
Research Sites
213 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to understand the cause of adverse events in patients treated with phage therapy for bone, joint, or implant infections. The study investigates whether these adverse effects are related to surgery, antibiotic treatment, or the phage therapy itself. It is an observational study led by Hospices Civils de Lyon. Patients included in this study are those who have experienced an adverse event after receiving phage therapy for their infection. The study does not involve new treatments or interventions but observes and collects data on past adverse events associated with phage therapy, surgery, or antibiotic use. Participants' medical records will be reviewed to identify the rate and types of adverse events occurring within one year after treatment. The study will assess which events are linked specifically to surgery, antibiotic therapy, or phage therapy. This information will help researchers understand the safety profile of phage therapy in these infections.
CONDITIONS
Brief Title
Phage Safety Retrospective Cohort Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients having had a bone, joint, or implant infection treated by phagotherapy
- Patients having experienced an adverse event after phagotherapy
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - 1 year
Participants who have had phagotherapy for bone, joint, or implant infection and experienced adverse events are observed to assess the rate and type of adverse events over time.
Trial Site Locations
Total: 1 location
1
Hospices Civils de Lyon
Lyon, France, 69004
Actively Recruiting
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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