Impact of Dexmedetomidine on the Post-Operative Cognition Dysfunction(POCD) in Geriatric Patients

Sponsor
The First Affiliated Hospital of Anhui Medical University (Other)
Overall Status
Completed
CT.gov ID
NCT02275182
Collaborator
(none)
864
13
2
28.7
66.5
2.3

Study Details

Study Description

Brief Summary

Post-Operative Cognition Dysfunction (POCD) is a common complication after surgery, POCD can lead to a reduced ability and seriously affect the quality of life of patients, increase personal and social burden, POCD may also increase mortality.POCD can occur at any age, but the long-term, affect the daily lives of POCD in elderly patients over 60 years of age are more prone. Age is a risk factor for advanced or long-term POCD. POCD determined by preoperative cognitive function and psychological scales postoperative assessment, the main recommendation of the agreed test methods include, Rey auditory verbal test, the connection test, digit span test. In this study, preoperative mini-mental state examination (MMSE) screening, comprehensive neurological function during hospitalization for memory, attention, executive function and exercise capacity test, and telephone follow-up after discharge Scale Revised (TICS-M) test.

Few study showed that dexmedetomidine may improve cognitive function in young patients others show that dexmedetomidine did not reduce POCD incidence after 24 hours of surgery. These results conflict and it is necessary to carry out large-scale, multi-center, randomized, controlled clinical study to determine whether dexmedetomidine reduce the POCD incidence or not for elderly patients.

Condition or Disease Intervention/Treatment Phase
Phase 4

Study Design

Study Type:
Interventional
Actual Enrollment :
864 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Impact of Dexmedetomidine Sedation on the Post-Operative Cognition Dysfunction--a Multiple Center,Randomized, Controlled,Double Blinded Clinical Trial.
Actual Study Start Date :
Oct 1, 2014
Actual Primary Completion Date :
Jan 1, 2017
Actual Study Completion Date :
Feb 20, 2017

Arms and Interventions

Arm Intervention/Treatment
Experimental: Dexmedetomidine

0.5μg/kg Dexmedetomidine as initial loading dose is given for 15 minutes before induction of anesthesia, followed by a maintenance infusion of 0.4μg/kg/h and stopped 30 minutes before the surgery over.

Drug: Dexmedetomidine
0.5μg/kg Dexmedetomidine as initial loading dose is given for 15 minutes before induction of anesthesia, followed by a maintenance infusion of 0.4μg/kg/min and stopped 30 minutes before the surgery over.
Other Names:
  • Yisi
  • Placebo Comparator: Controlled

    0.5μg/kg Saline as initial loading dose is given for 15 minutes before induction of anesthesia, followed by a maintenance infusion of 0.4μg/kg/h and stopped 30 minutes before the surgery over.

    Drug: Saline
    0.5μg/kg saline as initial loading dose is given for 15 minutes before induction of anesthesia, followed by a maintenance infusion of 0.4μg/kg/min and stopped 30 minutes before the surgery over.

    Outcome Measures

    Primary Outcome Measures

    1. The change of incidence of postoperative cognition dysfunction [1 day Before surgery,the 3rd,7th day after the surgery.]

      The neuropsychological tests performed at the day before the surgery, the 3rd and 7th day after the surgery respectively. A test environment to keep quiet, well-lit, non-interference, all the test items should be completed within 30 min. Normal population (65 to 90 years age-matched 400 non-surgery people) should perform neuropsychological tests in the same time interval, then calculate the score difference(ΔXc), and the standard deviation(SD) of the difference. Calculate the difference(ΔX) between the score obtained before surgery and 3 or 7 days after the surgery (there are both positive and negative, we use the absolute value), with this difference( ΔX) divided by the standard deviation(SD)of the difference of the normal population, that is ΔX / SD and it is the Z score. POCD Diagnosis: if a patient has two or more than two of the absolute value of Z scores ≥1.96, the POCD is exist.

    2. The change of incidence of postoperative delirium [The first, second and third day after the surgery.]

      Through CAM-ICU to assess the incidence of the postoperative delirium.

    3. The change of Neuropsychological status [the 3rd,6th month after the surgery]

      Through the Telephone Interview for Cognitive Status-Modified(TICS-m) to follow up.

    Secondary Outcome Measures

    1. The occurrence of cardiovascular events. [from begging of the anesthesia to the time the patients discharge, up to 1 month.]

    2. The incidence of any adverse or severe adverse events. [From the beginning of the admitted to 6 month after the surgery, up to 6 month.]

      Including kidney or brain related adverse events.

    3. The variation of heart rate. [From the beginning to the end of anesthesia,up to 6 hours.]

      Heart rate is recorded every 15 minutes during the anesthesia.

    4. The variation of blood pressure. [From the beginning to the end of anesthesia,up to 6 hours.]

      blood pressure is recorded every 15 minutes during the anesthesia.

    5. the variation of pulse oxygen saturation. [From the beginning to the end of anesthesia,up to 6 hours.]

      Pulse oxygen saturation is recorded every 15 minutes during the anesthesia.

    6. The monitor of depth of anesthesia. [From the beginning to the end of anesthesia,up to 6 hours.]

      Bispectral index (Bis) is recorded every 15 minutes during the anesthesia.

    7. The serum concentrations of BDNF [From the baseline to the 3-day,7-day and 1-month.]

      Serum level of brain-derived neurotrophic factor (BDNF) was measured

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    65 Years to 90 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    1. Written informed consent

    2. Selective surgery and general anesthesia patients(abdomen,orthopedics and urology surgery is preferred);

    3. Age 65-90 yrs;

    4. Anesthesia Society of American (ASA) Scale II~III;

    5. Anticipated surgery time 2-6 hrs; -

    Exclusion Criteria:
    1. Dementia patients(Mini-mental state examination< 20)

    2. Factors existed that affect cognition assessment such as language,visual,and auditory dysfunction;

    3. Unstable metal status and mental disease;

    4. The cognitive function examination in 3-6 months is not anticipated to be completed

    5. II-III Atrioventricular block;

    6. Heat rate < 50 beats/minutes;

    7. Parkinson's Disease;

    8. May occur or have occurred the difficult airway or anticipated delayed extubation

    9. Sure or suspected abuse of analgesic and sedation drug;

    10. Allergic to the trial drug and other anesthesia drug contraindication; -

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Anqing Municipal Hospital Anqing Anhui China
    2 Affiliated Hospital of Bengbu Medical College Bengbu Anhui China
    3 Affiliated Chaohu Hospital of Anhui Medical Hospital Chaohu Anhui China
    4 Binhu Hospital of Hefei Hefei Anhui China
    5 Second Affiliated Hospital of Anhui Medical University Hefei Anhui China
    6 The First Affiliated Hospital of Anhui Medical University Hefei Anhui China
    7 The first Hospital of Hefei Hefei Anhui China
    8 The Second Hospital of Hefei Hefei Anhui China
    9 The Second People's Hospital of Anhui Hefei Anhui China
    10 the people's Hospital of Liuan Liuan Anhui China
    11 the people's Hospital of Tongling Tongling Anhui China
    12 The First Affiliated Hospital of Wannan Medical College Wuhu Anhui China
    13 The second People's Hospital of Wuhu Wuhu Anhui China

    Sponsors and Collaborators

    • The First Affiliated Hospital of Anhui Medical University

    Investigators

    • Principal Investigator: Wei Er Gu, The First Affiliated Hospital of Anhui Medical University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Xinqi Cheng, Anesthesia Department, The First Affiliated Hospital of Anhui Medical University
    ClinicalTrials.gov Identifier:
    NCT02275182
    Other Study ID Numbers:
    • 201401
    First Posted:
    Oct 27, 2014
    Last Update Posted:
    Apr 25, 2018
    Last Verified:
    Apr 1, 2018
    Keywords provided by Xinqi Cheng, Anesthesia Department, The First Affiliated Hospital of Anhui Medical University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 25, 2018