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Epidemiology, Risk Factors, and Outcomes of Infections of Lower Limb MEGAprostheses

Epidemiology, Risk Factors, and Outcomes of Infections of Lower Limb MEGAprostheses

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07544212
Acronym
EROMEGA
Enrollment
200
Registered
2026-04-22
Start date
2025-12-10
Completion date
2026-08-31
Last updated
2026-06-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lower Limb Megaprosthetis Infection

Keywords

Megaprosthetic Joint Infection, DAIR, MPJI, PJI, Prosthetic Joint Infection

Brief summary

Retrospective, multicenter, non-profit observational study. The study will include consecutive patients who underwent lower-limb megaprosthesis implantation at the participating Centers between January 1, 2020, and June 30, 2023.

Detailed description

Megaprostheses are large orthopedic prostheses used to replace extensive portions of bone and joints, typically after the removal of bone tumors or in other conditions involving major bone loss (severe trauma, revisions). In the 1990s, they became the standard for reconstruction following resection of primary malignant bone tumors. Over time, the indications for the use of megaprostheses have expanded to include benign but locally aggressive bone tumors, bone metastases, and malignant soft tissue tumors. Currently, the number of megaprosthesis procedures for non-oncologic conditions is also increasing. The anatomical sites where a megaprosthesis can be implanted include the femur (proximal, distal, or total), the proximal tibia, and the proximal humerus. Megaprostheses are modular metal structures (titanium, chrome-cobalt) that may include an artificial bone segment, a joint component (hip, knee, shoulder), and potentially an antibacterial coating (such as silver). While a megaprosthesis represents an important therapeutic option for limb salvage, it also involves complex surgery with significant complication and failure rates. Periprosthetic infection, with incidence rates ranging from 3% to 30%, is certainly one of the most feared complications, as it is associated with increased morbidity and mortality, longer patient recovery times, and higher healthcare costs. Revising a megaprosthesis often presents additional technical challenges for orthopedic surgeons (for example, the impossibility of replacing the implant due to the lack of remaining tissues). Moreover, the rate of infectious complications in megaprostheses is higher than that of periprosthetic infections in standard joint replacements. Possible explanations include longer surgical times, greater soft tissue trauma, or patient-related factors (such as immunocompromised status in oncologic patients). The use of megaprostheses to treat different types of lower-limb conditions is increasing, and these prostheses carry a higher risk of infection compared to standard implants. There is a shortage of studies in the literature that specifically and thoroughly analyze risk factors for megaprosthesis infections, and existing studies often involve small patient cohorts. It is therefore highly rational to identify specific infection risk factors for patients receiving a lower-limb megaprosthesis, if present, to highlight those that may be modifiable and ultimately reduce the infection risk for individual patients. The primary objective of the study is to identify risk factors for the development of infection in lower-limb joint megaprostheses within 2 years of implantation.

Interventions

None listed

Sponsors

IRCCS Azienda Ospedaliero-Universitaria di Bologna
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
14 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

* Age ≥ 14 years * Implantation of a lower-limb megaprosthesis at one of the participating centers between January 1, 2020, and June 30, 2023 * At least 2 years of follow-up after megaprosthesis implantation * Signed informed consent

Exclusion criteria

* None

Design outcomes

Primary

MeasureTime frameDescription
Percent of patients with and without a diagnosis of megaprosthesis infection24 months after prosthesis placementDistribution of the study variables in the two groups of patients with and without megaprosthesis infection

Secondary

MeasureTime frame
Number of patients diagnosed with lower-limb megaprosthesis infection / number of patients who received a lower-limb megaprosthesis24 months after prosthesis placement
Sex, Charlson index, indication for prosthesis placement, symptoms and etiology of the infection in patients diagnosed with megaprosthesis infectionDuring prosthesis placement procedure and at the time of diagnosis of the megaprosthesis infection (assessed up to 2 months after prosthesis placement)
Age of patients diagnosed with megaprosthesis infectionDuring prosthesis placement procedure and at the time of diagnosis of the megaprosthesis infection (assessed up to 2 months after prosthesis placement)
Number and type of surgical procedures performed for the treatment of megaprosthesis infectionWithin 24 months after prosthesis placement
Sex of patients diagnosed with megaprosthesis infectionDuring prosthesis placement procedure and at the time of diagnosis of the megaprosthesis infection (assessed up to 2 months after prosthesis placement)
Number and type (molecule(s), route of administration, dosage, duration) of antibiotic treatments prescribed for the treatment of megaprosthesis infectionWithin 24 months after prosthesis placement
Percent of patients with megaprosthesis infection who experience clinical failure24 months after prosthesis placement
Charlson index in patients diagnosed with megaprosthesis infectionDuring prosthesis placement procedure and at the time of diagnosis of the megaprosthesis infection (assessed up to 2 months after prosthesis placement)

Countries

Italy

Contacts

CONTACTSARA TEDESCHI
sara.tedeschi5@unibo.it+39 051 2143353
PRINCIPAL_INVESTIGATORSARA TEDESCHI

IRCCS Azienda Ospedaliero-Universitaria di Bologna

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 13, 2026