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Clinical Trials/NCT04755686
NCT04755686
Withdrawn
Not Applicable

Effects of Fast-tracking Hip Fracture Patients in Geriatric Medicine Wards on Complication Incidence and Time of Hospitalization

Sahlgrenska University Hospital, Sweden1 site in 1 countryJune 2013
ConditionsHip Fracture

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hip Fracture
Sponsor
Sahlgrenska University Hospital, Sweden
Locations
1
Primary Endpoint
Incidence of complications (composit endpoint of non-fatal major bleeding, pressure ulcer, non-fatal infections, confusion, non-fatal tromboembolic events, all-cause mortality)
Status
Withdrawn
Last Updated
5 years ago

Overview

Brief Summary

The purpose of this study is to determine whether fast-tracking hip fracture patients to geriatric medicine wards, as opposed to standard care at the emergency room, results in less complications and shorter hospitalization for the patients.

Detailed Description

Each year about 18000 persons in Sweden suffer from a hip fracture. These people are often among the oldest and have many complicating diseases. The one-year mortality after hip fracture is 20%. Due to the complexity including many comorbidities in these patients, it is of great value that the care of these patients is optimal. Today, most of the patients with suspected hip fracture in the catchment area of Sahlgrenska University hospital, Gothenburg, are transported directly to the radiology unit. Thereafter, the patient waits in the emergency room (ER) for an othopedic examination before being admitted to primarily a geriatric medicine ward where they wait for the operation. The average waiting time in the ER is today around four hours. The current scientific evidence for fast-tracking hipfracture patients is limited. The aim of our randomized controlled trial is to determine the effect of fast-tracking hip fracture patients at geraitric medicine wards compared to standard care regarding complication rate (primary endpoint), lenght of hospital stay and time to operation (secondary outcomes).

Registry
clinicaltrials.gov
Start Date
June 2013
End Date
June 2017
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Sahlgrenska University Hospital, Sweden
Responsible Party
Principal Investigator
Principal Investigator

Mattias Lorentzon

Associate Professor, MD, PhD

Sahlgrenska University Hospital, Sweden

Eligibility Criteria

Inclusion Criteria

  • patients with low energy trauma with pain at the hip and/or groin AND
  • respiratory frequency: 8-25/minute AND
  • saturation: 90% or higher on air AND
  • pulse: 50-119 beats per minute AND
  • systolic blood pressure: \>90 mmHg AND
  • level of consciousness: Reaction level scale (RLS) 1 or Glasgow Coma Scale (GCS) 14-15 AND
  • plasma-glucose: 3,0-25 mmol/l

Exclusion Criteria

  • We will exclude patients based on the following criteria:
  • distal status affected
  • suspicion of other simultaneous fracture
  • suspicion of head trauma or affected consciousness
  • suspicion of acute cardiac disease
  • signs of acute cardiac ischemia in electrocardiogram
  • generalized symtoms, except for pain in the hip

Outcomes

Primary Outcomes

Incidence of complications (composit endpoint of non-fatal major bleeding, pressure ulcer, non-fatal infections, confusion, non-fatal tromboembolic events, all-cause mortality)

Time Frame: at time of discharge from geriatric medicine ward, after four months and after one year

Secondary Outcomes

  • Length of hospital stay, time to operation, all-cause mortality, functional ability after discharge, proportion of patients returning to former living, self assessed health status(At time of discharge from geriatric medicine ward, after four months and after one year)

Study Sites (1)

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