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. 2019 Apr 23;13:1301–1310. doi: 10.2147/DDDT.S194894

Table 1.

Main characteristics of included studies

Reference Year Location Study design n Jaw Age, years (mean ± SD or range) Total surgery time, minutes (mean ± SD) Dexmedetomidine dosage Control (type) Evaluation indicator
Cheung et al26 2011 Hong Kong RCT (parallel) 60 Mand 27.1±6.2D
26.9±5.7P
25.6±13.6D
24.7±12.5P
1.0 μg/kg 0.9% saline OAA/S, BIS, pain, HR, SBP
Gu et al27 2014 Nanjing, China RCT (parallel) 30 Mand 25–35 27±6D
28±7P
1.5 μg/kg 0.9% saline OAA/S, HR, SBP
Nooh et al25 2013 Riyadh, Saudi Arabia RCT (split mouth) 18 Mand 25±3.9 28±9D
30±7P
1.5 μg/kg Water OAA/S, BIS, pain, HR, SBP
Ryu et al24 2016 Seoul, South Korea RCT (parallel) 240 Mand 26.0±8.1D
25.6±1.6P
20.1±10.3D
20.3±11.5P
1.5 μg/kg No treatment Pain, adverse events, patient satisfaction, and BIS
Shetty and Aggarwal23 2016 Mysore, India RCT (split mouth) 15 Mand 18–35 NR 1.5 μg/kg 0.9% saline OAA/S, pain

Notes:

D

Dexmedetomidine;

P

placebo. Dexmedetomidine administered intranasally.

Abbreviations: RCT, randomized controlled trial; Mand, mandibular third molar surgery; OAA/S, observer assessment of alertness/sedation; BIS, bispectral index; HR, heart rate; SBP, systolic blood pressure; NR, not reported.