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Not yet recruiting NCT07132723

Associations Between Time to Reduction and Complications in Patients With Dislocated Total Hip Arthroplasty

Observational Closed Reduction Arthroplasty, Replacement, Hip Length of Stay

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Time in minutes from admission to closed reduction.
Who it may be relevant to
Registry conditions: Closed Reduction, Arthroplasty, Replacement, Hip, Length of Stay. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Denmark
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Associations Between Time to Reduction and Complications in Patients With Dislocated Total Hip Arthroplasty - A Protocol for an Observational Cohort Study

Overview

The aim of the study is to investigate the impact of time to closed reduction on both patient related and organizational factors. These include, length of stay, hospitalization, admission to intensive care unit, rehospitalizations, delirium, all-cause mortality, infection requiring hospital contact, and cardiovascular complications. It is also intended to investigate whether different anaesthetic strategies and airway management are associated with different complication rates. It is hypothesized that longer waiting time until reduction increase the postoperative length of stay, readmissions, and risk of complications.

Interventions

  • Other Time in minutes from admission to closed reduction
    Time in minutes from admission to closed reduction measured as: From arriving time in the emergency department until the start of surgery in the operating theater.

Primary outcome measures

  • Post procedure length of stay [Time frame: 30 days after the closed reduction]
Secondary outcome measures (7)
  • All-cause mortality [Time frame: 90 days after closed reduction]
  • Admissions to Intensive care unit [Time frame: 30 days after the closed reduction]
  • Readmission [Time frame: 30 days after discharge]
  • Delirium during admission [Time frame: From admission to discharge up to 30 days after closed reduction]
  • Acute kidney failure [Time frame: Post procedure until 30 days after discharge]
  • Infection requiring hospital contact [Time frame: Post procedure until 30 days after discharge]
  • Cardiovascular complications [Time frame: From admission to 30 days after discharge.]

Eligibility criteria

Inclusion criteria

Patients will be considered eligible for inclusion if they meet all of the following criteria:

  • Aged 18 years or older
  • Presented to the emergency department with a dislocated total hip arthroplasty.
  • Undergo closed reduction of the dislocated total hip arthroplasty in the operating theatre, with the involvement of the Department of Anesthesiology.

Exclusion criteria

  • Were primarily booked for open surgical reduction.
  • Did not have a complete case log (i.e. time of admission; referral to the operation theatre; anesthesia induction; discharge, etc.) and we were unable to recreate the log using simple code rules.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

Denmark · 1 center
  • Department of Anesthesiology, North Zeeland Hospital — Hillerød

Identifiers

NCT: NCT07132723 · HIP_REDUCTION

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗