Overview
Study of Cisatracurium and Sufentanil Consumption Using a Closed Loop Computer Control Infusion System
Status:
Unknown status
Unknown status
Trial end date:
1969-12-31
1969-12-31
Target enrollment:
0
0
Participant gender:
All
All
Summary
The purpose of this study is to: - determine the effect of dexmedetomidine on cisatracurium infusion requirements and sufentanil consumption. - analyze the cisatracurium infusion requirements and sufentanil consumption in different age groups.Phase:
N/AAccepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
Tianjin Medical University General HospitalCollaborators:
Donglai Yan
Haiyun Wang
Shehzaad JoomyeTreatments:
Atracurium
Cisatracurium
Dexmedetomidine
Dsuvia
Sufentanil
Criteria
Inclusion Criteria:- ASA status 1 and 2.
- Consent approval written and oral.
- Patients scheduled for elective abdominal surgery under general anesthesia.
Exclusion Criteria:
- Patients with neuromuscular disorders.
- Patients with history of stroke, flaccid paralysis or other neurological disorders.
- Significant renal, hepatic or cardiac dysfunction.
- Consent refusal.