Treatment of Osteomyelitis-associated Pressure Ulcers by Surgical Flaps and Anti-bacterial Agents
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorInstitut de Sante Parasport Connecte Synergies
About this trial
People with neuromotor disability (i.e. following an inborn or acquired spinal cord, cerebral or peripheral neurological lesion) are at high risk of osteomyelitis-associated pressure ulcers.
The management of osteomyelitis-associated pressure ulcers is controversial. In our center, patients benefit from a one stage surgical management with bone shaving and flap covering osteitis of pressure ulcer to perform wound closing. Surgery is followed by an antibiotic treatment, secondarily adapted to intraoperative samples.
The aim of this study is to describe the cohort and to identify factors associated with failure (or success) in this frail population.
Eligibility criteria
Qualifiers
Patients >= 18 years old ;
Treated in the Perioperative Disability Unit (UPOH) of the Physical Medicine and Rehabilitation Department of our university hospital;
Admitted for the treatment of an osteomyelitis-associated pressure ulcer by surgical flap;
Having a neuromotor disability;
Disqualifiers
Under court protection.
Trial design
Treatments tested in this trial
- Surgical flap and anti-bacterial agents
Treatment groups
400 Participants
are divided into 1 treatment groupSponsors and collaborators
Institut de Sante Parasport Connecte Synergies
Lead sponsor
Assistance Publique - Hôpitaux de Paris
Collaborator
Source ClinicalTrials.gov