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临床试验/CTRI/2026/02/103591
CTRI/2026/02/103591尚未招募不适用

Preoperative assessment of frailty as predictor of perioperative outcome in form of hospital length of stay in elderly patients undergoing major orthopaedic surgeries

Dr. Sujeet Rai1 个研究点 分布在 1 个国家目标入组 196 人开始时间: 2026年2月24日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
196
试验地点
1

研究概览

简要总结

Research hypothesis

The implementation of the Vulnerable Elders Survey 13 (VES 13) frailty tool in the

preoperative assessment of geriatric surgical patients effectively identifies individuals at

increased risk of adverse postoperative outcomes. It is hypothesized that patients with a

VES-13 score more than equal to 3 will have a significantly higher incidence of postoperative

complications, prolonged hospital stay, and non-home discharge compared to those with

lower scores, enabling early risk stratification and targeted interventions. Aim: Assessment of the effect of frailty on perioperative outcomes in elderly patients

undergoing major orthopaedic

Primary objective

To assess the effect of Frailty on perioperative outcome, in the form of hospital length of

stay on elderly patients undergoing major orthopaedic surgical procedures at Dr.

RMLIMS, Lucknow

Secondary objective

To assess the effect of frailty on intra-op and post-op complications like post-op

requirement of mechanical ventilation, requirement of vasopressors

To assess the association with ASA grading

To assess the association of frailty with 30 day mortality

Primary outcome measures included

Postoperative outcome in form of increased hospital length of stay

Postoperative complications (e.g., infection, wound dehiscence, reoperation, ICU

transfer)

Discharge disposition (home, rehabilitation, or extended care)

In-hospital mortality.

Secondary outcomes included

Correlation between VES-13 scores and ASA grade,

Need for postoperative ICU admission,

Functional decline at discharge.

Significance of the study

By doing the study, we can assess beforehand which patients are going to stay longer in

the hospital, or have more days on mechanical ventilation, and have more chances of

complications or mortality, so we are able to prognosticate the patient pre-operatively.

研究设计

研究类型
Observational

入排标准

年龄范围
65.00 Year(s) 至 99.00 Year(s)(—)
性别
All

入选标准

  • Patients give consent for the study Age more than equal to 65 years Undergoing any major elective surgical procedure.

排除标准

  • Refused to give consent for the study Patients with severe cognitive impairment Patients who are critically ill and unable to participate.

研究者

发起方
Dr. Sujeet Rai
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Dr Sujeet Rai

DrRMLIMS LUCKNOW

研究点 (1)

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