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Inflammatory Indices, Early Mortality, and ICU Stay in Geriatric PFN Patients

Study acronym: PFN-RAR
StatusCompleted
PhaseNot specified
Started
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Record History

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  1. Trial completed
    • Primary completion date changed from estimate of Jun 15, 2026 to Dec 1, 2025
    • Study completion date changed from estimate of Jun 30, 2026 to Dec 30, 2025
    • Eligibility criteria expanded, about 15 words
  2. Re-verified, no change to tracked fieldsv2
  3. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
This retrospective observational cohort study aims to evaluate the association between preoperative and postoperative inflammatory indices and early postoperative outcomes in geriatric patients undergoing proximal femoral nailing (PFN) for intertrochanteric femur fractures. The primary outcome of the study is 30-day mortality, while the secondary outcome is intensive care unit (ICU) length of stay. Various inflammatory biomarkers derived from routine laboratory parameters, including neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), monocyte-to-lymphocyte ratio (MLR), systemic immune-inflammation index (SII), systemic inflammation response index (SIRI), immune-inflammatory prognostic index (IPI), aggregate index of systemic inflammation (AIS), and RDW-to-albumin ratio (RAR), will be analyzed to investigate their prognostic value in the acute postoperative period. The study seeks to identify simple and readily accessible biomarkers that may contribute to early risk stratification and perioperative management in elderly hip fracture patients.
Trial Details
NCT Number NCT07607886
Lead Sponsor Saglik Bilimleri Universitesi
Conditions
(from sponsor)		 Intertrochanteric Femur Fracture, Hip Fracture Surgeries, Geriatric Anesthesia
Enrollment 233 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov