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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03393676
Other study ID # PPOCD20161201
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 10, 2018
Est. completion date March 31, 2020

Study information

Verified date March 2020
Source RenJi Hospital
Contact Xiaorong Huai, MS
Phone 13818003683
Email smile_huai@126.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to investigate whether preoperative pain is the risk factor of POCD in elder patients.


Description:

Postoperative cognitive dysfunction (POCD) occurs mainly in aged patients. The mechanism of POCD is not clear yet and no effective therapy method. In the present study, we conducted a single-center observational prospective cohort trial in elder patients who undergoing hip joint replacement surgery with general anesthesia to test our hypothesis that preoperative chronic pain is one of the risk factors of POCD after major joint replacement surgery.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date March 31, 2020
Est. primary completion date March 31, 2020
Accepts healthy volunteers No
Gender All
Age group 65 Years and older
Eligibility Inclusion Criteria:

1. Elder than 65 years old

2. Speak Chinese Mandarin

3. Those who will undergo major low limb surgery like hemiarthroplasty or total hip arthroplasty with general anesthesia.

4. Signed the inform consent

5. American Society of Anesthesiologists classification I to II

Exclusion Criteria:

1. Existing cerebral disease, or have a history of neurological and psychiatric disease including Alzheimer Disease, stroke, epilepsy and psychosis

2. Existing cognitive impairment as evidenced by Mini-Mental State Examination scores below 24

3. Severe hearing or visual impairment

4. Unwillingness to comply with the protocol or procedures

5. Cannot communicate with Chinese Mandarin

6. Serious pulmonary, heart , liver or renal insufficiency patients

7. Had anesthesia or surgery within the past 30 days

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
China Reni Hospital, Shanghai Jiao Tong University, School of Medicine Shanghai Shanghai
China Shanghai Ren ji Hospital Shanghai Shanghai

Sponsors (1)

Lead Sponsor Collaborator
RenJi Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary POCD incidence 7 days (or before leaving hospital) after surgery POCD incidence 7 days (or before leaving hospital) after surgery 7 days (or before leaving hospital)
Secondary POCD incidence 2 months after surgery POCD incidence 2 months after surgery 2 months after surgery
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