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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04216615
Other study ID # XYFY-2019-0156
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date January 4, 2020
Est. completion date October 1, 2020

Study information

Verified date December 2019
Source Xuzhou Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Postoperative delirium is a common and important complication in patients. The aim of this study was to investigate whether preoperative anxiety predicted onset of postoperative delirium in elderly patients undergoing orthopaedic surgery, so as to help develop preventive approaches.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 290
Est. completion date October 1, 2020
Est. primary completion date September 1, 2020
Accepts healthy volunteers
Gender All
Age group 65 Years and older
Eligibility Inclusion Criteria:

- aged 65 or older

- patients undergoing elective orthopaedic surgery

- ASA I-III

Exclusion Criteria:

- history of craniocerebral trauma surgery or severe central nervous system disease

- inability to read or understand the informed consent documents

- too physically or psychologically ill

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
preoperative anxiety
patients who are anxious

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Xuzhou Medical University

Outcome

Type Measure Description Time frame Safety issue
Primary Incidence of postoperative delirium postoperative delirium is diagnosed using CAM 5-day postoperative period
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