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Preoperative Pain and POCD in Elderly Patients

Unknown statusNCT03393676
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

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

Study details

Official title
Preoperative Chronic Pain Increases the Risk of Early Postoperative Cognitive Dysfunction in Elderly Patients Undergoing Hip Joint Replacement Surgery: a Prospective Observational Cohort Study
Conditions
  • Postoperative Cognitive Dysfunction
Sponsor
RenJi Hospital
Start date
2018-01-10
Primary completion
2020-03-31
Sex
All
Age range
from 65 Years
Results posted
No results posted in this snapshot
Countries
China
Total sites listed
2

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
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

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT03393676