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Effects of Fast-tracking Geriatric Hip Fracture Patients

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

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04755686
Enrollment
0
Registered
2021-02-16
Start date
2013-06-30
Completion date
2017-06-30
Last updated
2021-02-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hip Fracture

Keywords

hip fracture, fast-tracking, complications

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).

Interventions

PROCEDUREFast-tracking

Sponsors

Sahlgrenska University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
Incidence of complications (composit endpoint of non-fatal major bleeding, pressure ulcer, non-fatal infections, confusion, non-fatal tromboembolic events, all-cause mortality)at time of discharge from geriatric medicine ward, after four months and after one year

Secondary

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

Countries

Sweden

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026