Naples Prognostic Score for Predicting Postoperative Delirium
1 other identifier
observational
168
1 country
1
Brief Summary
Naples Prognostic Score (NPS) originally developed to predict outcomes in inflammatory and malignant conditions; we asked if it can effectively predict postoperative delirium (POD) in elderly patients undergoing hip surgery? NPS integrate markers such as albumin, neutrophil-to-lymphocyte ratio, and lymphocyte-to-monocyte ratio-all of which have been linked to adverse postoperative outcomes including POD.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Jan 2026
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
November 25, 2025
CompletedFirst Posted
Study publicly available on registry
December 22, 2025
CompletedStudy Start
First participant enrolled
January 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 1, 2027
January 5, 2026
December 1, 2025
1.4 years
November 25, 2025
December 30, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Assessment of postoperative delirium
Assessment of postoperative deliurim will be done once daily by using an established screening instrument (The Confusion Assessment Method (CAM)). A positive CAM requires both (1) Acute onset \& fluctuating course AND (2) Inattention, plus (3) Disorganized thinking OR (4) Altered level of consciousness.
on arrival to PACU, on postoperative day 1, 2, 3, 5, 7.
Secondary Outcomes (1)
Length of hospital stay
Directly before patients' discharge from hospital
Study Arms (1)
hip group
patients undergoing hip surgeries will be screened for delirium in the Post-Anesthesia Care Unit (PACU) on arrival, and once daily for the first 3 postoperative days (postoperative days 1 to 3), and on postoperative days 5 and 7.
Eligibility Criteria
elderly patients undergoing Hip fracture surgery
You may qualify if:
- The elderly age≥60 years
- American Society of Anesthesiologists (ASA) classification II∼IV
- Patients undergoing hip fracture surgery
- Patients who had a complete blood sample were taken preoperatively
You may not qualify if:
- Patient refused to participate and consent
- Patients with a history of mild cognitive impairment (MCI), dementia, and delirium
- Ptients with known preoperative infections (pulmonary infection, urinary infection, and sepsis).
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Qena University
Qina, Qena Governorate, 83511, Egypt
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- lecturer in anesthesia, Intensive Care and Pain Management
Study Record Dates
First Submitted
November 25, 2025
First Posted
December 22, 2025
Study Start
January 1, 2026
Primary Completion (Estimated)
June 1, 2027
Study Completion (Estimated)
December 1, 2027
Last Updated
January 5, 2026
Record last verified: 2025-12
Data Sharing
- IPD Sharing
- Will not share