NCT02670954

Evaluation of the Effect of Appropriate Sedation for Patients After Abdominal Surgeries : A Prospective Randomised Controlled Study

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 154 (actual)
• Sponsor: Chinese Medical Association · Network
• Sex: All
• Age: 16 Years – 85 Years
• Healthy volunteers: Not accepted

Summary

To evaluate the efficacy and safety of appropriate postoperative sedation with dexmedetomidine for patients after abdominal surgeries.Prospective randomised controlled study was conducted among patients after abdominal surgeries began in October 2015.The investigators enroll patients who received abdominal surgeries. One group receive sedative along with analgesic and the other group analgesic only for the other group on the first 24 hours after surgeries and will follow up for 3 days.

Conditions

• Postoperative Sedation, Abdominal Surgery

Interventions

Type	Name	Description
DRUG	Dexmedetomidine, tramadol and flurbiprofen
DRUG	tramadol and flurbiprofen

Timeline

• Start date: 2015-10-01
• Primary completion: 2015-12-01
• Completion: 2016-01-01
• First posted: 2016-02-02
• Last updated: 2016-02-02

Locations

1 site across 1 country: China