Actively Recruiting

Age: 65Years +
All Genders
ID06614478

Frailty in Hip Fracture Patients Treated With Surgery; the Role of Simple Inflammatory Biomarkers. An Observational Study

Led by University of Thessaly · Updated on 2026-05-05

200

Participants Needed

2

Research Sites

6 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Frailty is a common condition among elderly patients who have hip fractures and is linked to worse outcomes. Researchers are studying whether hip fracture patients who have frailty show higher levels of inflammation based on simple blood tests measuring inflammatory biomarkers. This observational study aims to understand the relationship between frailty and inflammation in this group of patients. The study observes hip fracture patients who are treated with surgery. Frailty will be assessed using the Groningen Frailty Indicator, a validated tool. No experimental treatments are given; rather, the study collects data on patients' frailty status and inflammatory markers before surgery to explore possible links. Participants will be evaluated before their surgery with assessments of their frailty status and blood tests for inflammatory biomarkers. Researchers will gather information on these markers and frailty to analyze potential associations. The study is observational, so patients continue their usual care while data is collected. Participation involves preoperative assessments with no additional treatments or interventions required.

CONDITIONS

Brief Title

Frailty, Hip Fractures and Inflammatory Biomarkers

Who Can Participate

Age: 65Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age greater than 65 years
  • ASA Physical Status classification I to III
  • Not living in an institution
  • Able to communicate effectively
  • Patients with hip fractures treated with surgery
Not Eligible

You will not qualify if you...

  • Severe cognitive dysfunction
  • Patients treated without surgery (conservatively)
  • Patients with pathological fractures
  • Patients who refuse to participate

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Diagnostic Evaluation

Duration - Preoperative period

Participants undergo assessments including frailty status and inflammatory biomarker measurements before surgery.

1 visit (in-person)

Surgery and Immediate Post-operative Care

Duration - Hospital stay duration

Participants receive surgery for hip fracture and immediate post-operative care.

Post-operative Follow-up

Duration - Up to study completion in 2027

Participants are monitored after surgery to observe recovery and outcomes related to frailty and inflammatory biomarkers.

Trial Site Locations

Total: 2 locations

1

Larissa University Hospital

Larissa, Thessaly, Greece, 41110

Actively Recruiting

2

UHL

Larissa, Thessaly, Greece, 41110

Actively Recruiting

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Research Team

E

Eleni Arnaoutoglou, Professor

M

Maria Ntalouka, MD, PhD, MSc

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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