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Clinical Trials/NCT04451538
NCT04451538
Terminated
Not Applicable

Impact of Perioperative Nutritional Intervention on Perioperative Outcomes of Elderly Patients Having Hip Fracture Surgery: A Randomized Control Trial

Peking University First Hospital3 sites in 1 country30 target enrollmentDecember 28, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Elderly Patients
Sponsor
Peking University First Hospital
Enrollment
30
Locations
3
Primary Endpoint
Incidence of delirium or non-delirium complications after surgery
Status
Terminated
Last Updated
9 months ago

Overview

Brief Summary

Hip fracture is one of the most frequently occurred injury in the elderly and usually requires surgical treatment. Malnutrition is common in elderly patients with hip fracture and is associated with worse outcomes. This study is designed to test the hypothesize that, in elderly patients with malnutrition or at risk of malnutrition and scheduled for hip-fracture surgery, perioperative nutritional intervention may reduce early complications and improve long-term survival.

Detailed Description

Elderly patients with hip fracture have a high rate of malnutrition. In a cohort study of hip fracture patients aged 70 years or older, 18.8% have malnutrition and 44.6% are at risk of malnutrition. Increasing evidence suggest that preoperative nutritional status has a significant impact on clinical outcomes of elderly patients following surgery. For example, preoperative malnutrition or risk of malnutrition is associated with increased delirium, increased non-delirium complications, prolonged hospital stay, high mortality, and even worse long-term survival after surgery. We speculate that perioperative nutritional intervention may reduce postoperative delirium and improve early and long-term clinical outcomes in elderly hip-fracture patients. The purpose of this study is to observe the effect of perioperative nutritional intervention on early postoperative delirium and complications as well as long-term survival in the patients with malnutrition or at risk of malnutrition who are scheduled for hip-fracture surgery.

Registry
clinicaltrials.gov
Start Date
December 28, 2020
End Date
April 2, 2021
Last Updated
9 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Dong-Xin Wang

Professor and Chairman, Department of Anesthesiology and Critical Care Medicine

Peking University First Hospital

Eligibility Criteria

Inclusion Criteria

  • Age ≥70 years old;
  • Hospitalized for hip fracture, scheduled to undergo hip-fracture surgery within 48 hours;
  • Classified as malnutrition or at risk of malnutrition according to the short form mini-nutrition assessment (MNA-SF);
  • Provide written informed consents.

Exclusion Criteria

  • Pathological fracture;
  • History of schizophrenia, epilepsy, Parkinson's disease, or myasthenia gravis before surgery;
  • Unable to communicate due to coma, severe dementia, or language barrier;
  • Unable to eat due to any disease in the gastrointestinal system;
  • Severe hepatic dysfunction (Child-Pugh class C), renal failure (requirement of renal replacement therapy), respiratory failure (requirement of respiratory support), cardiac insufficiency (New York Heart Association classification ≥IV), or American Socisty of Anesthesiologists classification ≥IV;
  • Preexisting organ injury before surgery (delirium, acute kidney injury, myocardial injury, etc.);
  • Other conditions that are considered unsuitable for study participation.

Outcomes

Primary Outcomes

Incidence of delirium or non-delirium complications after surgery

Time Frame: Up to 30 days after surgery

Delirium is assessed twice daily with Confusion Assessment Method (CAM) or CAM for the Intensive Care Unit (CAM-ICU) during the first 5 days after surgery. Non-delirium complications indicate newly occurred conditions (other than delirium) that are harmful to patients' recovery and required therapeutic intervention within 30 days after surgery.

Secondary Outcomes

  • Incidence of organ injury within 5 days after surgery(Up to 5 days after surgery)
  • Incidence of non-delirium complications after surgery(Up to 30 days after surgery)
  • Cognitive function at 30 days after surgery(At 30 days after surgery.)
  • Length of intensive care unit stay after surgery(Up to 30 days after surgery)
  • Length of hospital stay after surgery(Up to 30 days after surgery.)
  • Quality of life at 30 days after surgery(At 30 days after surgery.)
  • Intensive care unit admission after surgery(Within 24 hours after surgery)

Study Sites (3)

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