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. 2016 Feb 18;2016(2):CD010358. doi: 10.1002/14651858.CD010358.pub2
Type of study: randomized controlled trial, including factorial trial and cluster‐randomized, but not cross‐over, design (Y/N/UN)
 
Participants: adults undergoing abdominal surgery, open or laparoscopic (Y/N/UN)
 
Type of intervention: dexmedetomidine administered perioperatively and as the sole difference between the intervention group and the control group(s), or administered perioperatively as part of a factorial trial (Y/N/UN)
 
At least one of the following outcomes (underscore)
Dose of rescue opioid
Postoperative pain measured by VASa
Proportion of participants needing rescue analgesia
Time to first rescue analgesia
Postoperative sedation
Proportion of participants with nausea/vomiting or needing antiemetics
Time to first flatus/stool or proportion of participants with delay to first flatus/stool
Time to out‐of‐bed mobilization or proportion of participants with delay to out‐of‐bed mobilization
INCLUDE only if yes in all 4 categories (Y/N/UN)
 
EXCLUDE and record here the information to be inserted into ‘Table of excluded studies’
 
Notes