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Nutritional Status and Its Modifications After Hip Replacement

I

I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio

Status

Completed

Conditions

Hip Arthropathy
Malnutrition; Anemia
Frail Elderly Syndrome

Study type

Observational

Funder types

Other

Identifiers

NCT03981354
NUTRIANCA (PI: M Briguglio)
L4133 (Other Grant/Funding Number)

Details and patient eligibility

About

Data literature lacks of evidence concerning the variation of the nutritional status in patients undergoing hip surgery, thus preventing an effective application a nutritional support program. It is therefore necessary to start identifying the clinical steps (pre-operative and post-operative) that may be defined as critical control points for malnutrition. The observation should foresee the identification of nutritional status indicators, such as weight, hemoglobin, albumin, food intake, and others that might affect a proper recovery. This study aims to investigate the prognostic nutritional factors that might influence clinical outcomes, and their variation in relation to hospitalization and rehabilitation periods.

Full description

Data literature lacks of evidence concerning the variation of the nutritional status in patients undergoing hip surgery, thus preventing an effective application a nutritional support program. It is therefore necessary to start identifying the clinical steps (pre-operative and post-operative) that may be defined as critical control points for malnutrition. Patients undergoing hip surgery would be enrolled before the surgical operation and would be evaluated three times: preoperative, postoperative, and after discharge. The observation should foresee the identification of nutritional status indicators, such as weight, hemoglobin, albumin, food intake, and others that might affect a proper recovery. This study aims to investigate the prognostic nutritional factors that might influence clinical outcomes, and their variation in relation to hospitalization and rehabilitation periods.

Enrollment

60 patients

Sex

All

Ages

60 to 85 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • caucasian
  • arthroplasty intervention program with hip prosthesis placement
  • signature and acceptance of informed consent to collaborate in all the procedures necessary for the study

Exclusion criteria

  • heart failure stage III-IV
  • renal failure stage III-IV
  • actual cancer
  • past neurological disorders (including, but not limited to cerebral ischemia, cerebral haemorrhages, brain tumors, endocranial aneurysms)
  • neurodegenerative disorders (including, but not limited to Alzheimer's dementia, fronto-temporal dementia)
  • actual major psychopharmacological therapies
  • pregnancy certified by self-declaration
  • inability to adhere to the rehabilitation protocol or to carry out the controls
  • non-acceptance of informed consent
  • revision interventions
  • previously established and documented sleep disorders
  • shift or part-time worker

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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