Quality of Life Clinical Trial
Official title:
Impact of Perioperative Dexmedetomidine on Long-term Outcomes in Elderly Patients After Cardiac Surgery: 6-year Follow-up of a Randomized Controlled Trial
NCT number | NCT03289325 |
Other study ID # | 2016-1188 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | December 5, 2016 |
Est. completion date | May 3, 2022 |
Verified date | October 2023 |
Source | Peking University First Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
A retrospective study showed that intraoperative dexmedetomidine administration was associated with decreased risk of 1-year mortality after cardiac surgery. In a previous randomized controlled trial, 285 elderly patients undergoing cardiac surgery were randomized to receive either perioperative dexmedetomidine or placebo (normal saline) administration. The purpose of this 6-year follow-up study is to investigate whether perioperative dexmedetomidine can improve long-term outcomes in those recruited elderly patients after cardiac surgery.
Status | Completed |
Enrollment | 285 |
Est. completion date | May 3, 2022 |
Est. primary completion date | May 3, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 60 Years and older |
Eligibility | Inclusion Criteria: 1. Age of 60 years or older; 2. Scheduled to undergo cardiac surgery (coronary artery bypass graft and/or valve replacement surgery); 3. Provide written informed consents. Exclusion Criteria: Patients who meet any of the following criteria will be excluded. 1. Preoperative history of schizophrenia, epilepsia, Parkinson syndrome, or severe dementia; 2. Inability to communicate in the preoperative period because of severe visual/auditory dysfunction or language barrier; 3. History of brain injury or neurosurgery; 4. Preoperative sick sinus syndrome, severe bradycardia (HR < 50 bpm), second-degree or above atrioventricular block without pacemaker; 5. Severe hepatic dysfunction (Child-Pugh class C); 6. Severe renal dysfunction (requirement of renal replacement therapy); 7. Other conditions that are considered unsuitable for participation. |
Country | Name | City | State |
---|---|---|---|
China | Beijing Fuwai Hospital | Beijing | Beijing |
China | Peking University First Hospital | Beijing | Beijing |
Lead Sponsor | Collaborator |
---|---|
Peking University First Hospital | Chinese Academy of Medical Sciences, Fuwai Hospital |
China,
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* Note: There are 23 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Overall survival after surgery | Overall survival after surgery | Up to 6 years after surgery | |
Secondary | Major adverse cardiovascular events-free survival after surgery | Major adverse cardiovascular events include cardiovascular death, nonfatal myocardial infarction, nonfatal stroke, and myocardial revascularization. | Up to 6 years after surgery | |
Secondary | Hospital-free survival after surgery | Event indicates any medical condition that lead to hospitalization after surgery. | Up to 6 years after surgery | |
Secondary | Cognitive function in 6-year survivors after surgery | Cognitive function is assessed with Telephone Interview for Cognitive Status-Modified (TICS-M; scores range from 0 to 50, with higher score indicating better cognitive function). | At the 6th year after surgery | |
Secondary | Health related quality of life in 6-year survivors after surgery | Health related quality of life is assessed with the short-form 36-item health survey questionnaire (SF-36). The SF-36 scale measures eight aspects of health status, i.e., physical functioning, role physical, bodily pain, general health, vitality, social functioning, role emotional, and mental health. It also measures changes of subjective healthy status during the last year (reported health transition). The scores of the above 9 items are calculated separately with scores range from 0 to 100, with higher score indicating better quality. | At the 6th year after surgery |
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