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NCT02544906 Clinical Trial

Propofol Versus Dexmedetomidine for Prevention of Sevoflurane Agitation in Recipients of Living Donor Liver Transplantation

Liver Transplantation Clinical Trial

— Agitation  

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT02544906
Other study ID # LTx 7
Secondary ID
Status Not yet recruiting
Phase N/A
First received September 7, 2015
Last updated September 8, 2015
Start date September 2015
Est. completion date October 2016

Study information
Verified date September 2015
Source Mansoura University
Contact n/a
Is FDA regulated No
Health authority Egypt: Ministry of Higher Education
Study type Interventional

Clinical Trial Summary

The use of propofol or dexmedetomedine for prevention of sevofurane emergence agitation in LDLT recipients

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 120
Est. completion date October 2016
Est. primary completion date October 2016
Accepts healthy volunteers No
Gender Both
Age group 30 Years to 60 Years
Eligibility Inclusion Criteria:

- All recipients of living donor liver transplantation

Exclusion Criteria:

- patient refusal Allergy to either propofol or dexmedetomediene CNS disease

Study Design

Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Prevention

Related Conditions & MeSH terms

Intervention

Drug:
• Propofol
Infusion of propofol to prevent emergence agitation in liver transplanta recipients
• dexmedetomedine
Infusion of dexmedetomedine to prevent emergence agitation in liver transplanta recipients

Locations
Country Name City State
Egypt Mansoura university Mansoura Dkahleya

Sponsors (1)
Lead Sponsor Collaborator
AlRefaey Kandeel

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary incidence of emergence agitation in liver trasnplant recipients 24 hours Yes
See also
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