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UnknownNCT02674737

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

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
80 (estimated)
Sponsor
Chinese Medical Association · Network
Sex
All
Age
18 Years – 85 Years
Healthy volunteers
Not accepted

Summary

To evaluate the efficacy and safety of appropriate postoperative sedation with dexmedetomidine for patients after gastrectomy. Prospective randomised controlled study was conducted from October 2015 and December 2015 among patients after gastrectomy. The investigators are going to 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 follow up for 3 days.

Conditions

Interventions

TypeNameDescription
DRUGdexmedetomidine, tramadol and flurbiprofen
DRUGtramadol and flurbiprofen

Timeline

Start date
2016-01-01
Primary completion
2016-05-01
First posted
2016-02-04
Last updated
2016-02-04

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT02674737. Inclusion in this directory is not an endorsement.

Evaluation of the Effect of Appropriate Sedation for Patients After Gastrectomy: A Prospective Randomised Controlled Stu (NCT02674737) · Clinical Trials Directory