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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02197403
Other study ID # an00543
Secondary ID
Status Recruiting
Phase Phase 4
First received
Last updated
Start date December 2013
Est. completion date May 31, 2019

Study information

Verified date March 2019
Source Chonnam National University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

1. Adequate sedation with classical sedative agents, propofol

2. Sedation with propofol may induce paradoxical excitement response in heavy alcohol drinkers

3. Dexmedetomidine, α2 receptor agonist, may provide adequate sedation in heavy alcohol drinkers


Description:

1. Adequate sedation during surgery provide anxiolysis and comfort to patient. Insufficient sedation can't provide comfort to patient during surgery, otherwise excessive sedation can cause variable complications like respiratory depression or delayed awakening.

2. Dexmedetomidine is a centrally acting α2 receptor agonist that is increasingly being used as a sedative for MAC and intensive care with mechanical ventilated patients because of its analgesic properties, "cooperative sedation," and lack of respiratory depression.

3. Because of the different site of action between dexmedetomidine and propofol, we assumed that paradoxical excitement responses which appeared in heavy alcohol drinkers in midazolam or propofol-induced sedation might be less observed in dexmedetomidine-induced sedation.


Recruitment information / eligibility

Status Recruiting
Enrollment 110
Est. completion date May 31, 2019
Est. primary completion date May 31, 2019
Accepts healthy volunteers No
Gender All
Age group 19 Years to 65 Years
Eligibility Inclusion Criteria:

- 19~65 yr-old patients who is scheduled to undergo knee surgery with regional anesthesia

Exclusion Criteria:

- History of taking anxiolytics, hypnotics, antiepileptic drugs

- Abnormal liver function test (eg: Liver cirrhosis, elevated liver enzymes)

- History of allergic reaction with dexmedetomidine or propofol

- Contraindication with regional anesthesia

- American society of anesthesiologist Physical status III or IV

Study Design


Intervention

Drug:
Dexmedetomidine
200mcg in 50mL of normal saline 0.75mcg/Kg bolus injection in 10 minutes 0.1~1.0mcg/Kg infusion
Propofol
25~75mcg/kg/min continuous infusion

Locations

Country Name City State
Korea, Republic of Chonnam National University Hwasun Hospital Hwasun Jeollanamdo

Sponsors (1)

Lead Sponsor Collaborator
Chonnam National University Hospital

Country where clinical trial is conducted

Korea, Republic of, 

References & Publications (4)

Adams R, Brown GT, Davidson M, Fisher E, Mathisen J, Thomson G, Webster NR. Efficacy of dexmedetomidine compared with midazolam for sedation in adult intensive care patients: a systematic review. Br J Anaesth. 2013 Nov;111(5):703-10. doi: 10.1093/bja/aet1 — View Citation

Candiotti KA, Bergese SD, Bokesch PM, Feldman MA, Wisemandle W, Bekker AY; MAC Study Group. Monitored anesthesia care with dexmedetomidine: a prospective, randomized, double-blind, multicenter trial. Anesth Analg. 2010 Jan 1;110(1):47-56. doi: 10.1213/ane — View Citation

Jakob SM, Ruokonen E, Grounds RM, Sarapohja T, Garratt C, Pocock SJ, Bratty JR, Takala J; Dexmedetomidine for Long-Term Sedation Investigators. Dexmedetomidine vs midazolam or propofol for sedation during prolonged mechanical ventilation: two randomized c — View Citation

Jeong S, Lee HG, Kim WM, Jeong CW, Lee SH, Yoon MH, Choi JI. Increase of paradoxical excitement response during propofol-induced sedation in hazardous and harmful alcohol drinkers. Br J Anaesth. 2011 Dec;107(6):930-3. doi: 10.1093/bja/aer275. Epub 2011 Se — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Paradoxical excitement response Paradoxical excitement responses (verbal/movement) 0, none : no excitement response
mild : increased talkativeness, irrational talking / brief spontaneous movement with position remaining
moderate : restlessness, loss of cooperation, spontaneous movements requiring repositioning with no need of restraint
severe : agitation and spontaneous movements with a need to restrain the patient
Every 5 minutes up to 120minutes after drug infusion
Secondary OAA/S Observer''s Assessment of Alertness/Sedation Scale (OAA/S)
:Does not respond to mild prodding or shaking
:Responds only after mild prodding or shaking
:Responds only after name is spoken loudly and/or repeatedly
:Lethargic response to name spoken in normal tone
:Responds readily to name spoken in normal tone
Goal to sedation : 3
Every 5minutes up to 120minutes after drug infusion
Secondary Vital signs Check blood pressure, heart rate, oxygen saturation, bispectral index During operation
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