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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01267786
Other study ID # AnesthSurg1
Secondary ID
Status Recruiting
Phase Phase 4
First received December 28, 2010
Last updated December 28, 2010
Start date December 2010

Study information

Verified date December 2010
Source Aretaieio Hospital
Contact Georgios P Fragulidis, MD
Phone +30 6072910955
Email gfragulidis@aretaieio.uoa.gr
Is FDA regulated No
Health authority Greece: Ethics Committee
Study type Interventional

Clinical Trial Summary

The aim of the study is to investigate the effect of sevoflurane and desflurane on hepatic function after ischemic/reperfusion injury and the sequence influence on renal and cardiovascular systems.


Recruitment information / eligibility

Status Recruiting
Enrollment 40
Est. completion date
Est. primary completion date December 2011
Accepts healthy volunteers No
Gender Both
Age group 30 Years to 80 Years
Eligibility Inclusion Criteria:

- Patients undergoing liver surgery

Exclusion Criteria:

- ASA IV, Cardiovascular diseases

Study Design

Allocation: Randomized, Endpoint Classification: Pharmacodynamics Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Basic Science


Related Conditions & MeSH terms


Intervention

Procedure:
Liver surgery
hepatectomy

Locations

Country Name City State
Greece Aretaieio Hospital Athens Attica

Sponsors (1)

Lead Sponsor Collaborator
Aretaieio Hospital

Country where clinical trial is conducted

Greece, 

Outcome

Type Measure Description Time frame Safety issue
Primary Oxidotic stress after hepatectomy. Perioperative liver and renal biopsies and follow up with liver renal function tests plus intraoperative and postoperative cardiovascular monitoring 5 d postop. Yes
Secondary Liver and renal dysfunction liver and renal impairment due to ischemic injury 5 d Yes
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