Prevention of Delirium Among Elderly Patients With Hip Fractures

NCT ID: NCT03470662

Last Updated: 2018-03-20

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

80 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-03-01

Study Completion Date

2017-09-30

Brief Summary

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Objective: To evaluate the effect of care bundle on prevention of delirium among elderly patients with hip fractures.

Methods: A prospective randomized case control study was performed for 80 patients (≥65 years) with hip fractures treated surgically according to their ages and the type of fractures from March 1th of 2017 to June 30th of 2017.There were 11 males and 69 females, with the age of (79.3±7.84) years. Confusion assessment method (CAM) was applied to diagnose delirium after surgery, the subjects were randomized divided into experimental group (n=43) and control group (n=37). The parameters next were recorded and analyzed, including age, gender, type of fractures, type of internal instrument, amount of bleeding, time between injured to surgery, time length of operation, type of operation, VAS, incidence of delirium, perioperative complications and adverse events.

Detailed Description

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Conditions

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Delirium Hip Fractures

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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experimental group

Care bundle

Group Type EXPERIMENTAL

Care bundle

Intervention Type OTHER

Care bundle

control group

routine care

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Care bundle

Care bundle

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* ≥65 years
* with hip fractures
* treated surgically

Exclusion Criteria

* \<65 years
* psychiatric history
* ICU post-operation
* refuse to join this study
* have delirium pre-operation
Minimum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Zhoupu Hospital, Pudong New Area, Shanghai, China

OTHER

Sponsor Role lead

Responsible Party

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Xiaoxiao Zhou

Director of Orthopaedics Department

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Zhoupu Hospital Shanghai

Shanghai, , China

Site Status

Countries

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China

Other Identifiers

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YuFengbinDelirium

Identifier Type: -

Identifier Source: org_study_id

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