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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00515905
Other study ID # StV 20-2004
Secondary ID
Status Completed
Phase N/A
First received August 13, 2007
Last updated September 14, 2010
Start date October 2004
Est. completion date September 2007

Study information

Verified date March 2008
Source University of Zurich
Contact n/a
Is FDA regulated No
Health authority Switzerland: Swissmedic
Study type Interventional

Clinical Trial Summary

One-lung ventilation; organ protection; volatile anesthetics

One-lung ventilation has become a common procedure for thoracoscopic surgery. Two hypothesis will be tested in this study:

1. Are inflammatory mediators increased in the re-ventilated lung after short-period pulmonary collapse?

2. Does Sevoflurane influence the production of inflammatory mediators in the re-inflated lung? Therefore, this study will elucidate the potential protective effect of a volatile anaesthetic (sevoflurane) on the production of inflammatory mediators by the respiratory compartment of the lung, i.e. the alveolar epithelium.

- Trial with immunomodulatory product / biological


Recruitment information / eligibility

Status Completed
Enrollment 76
Est. completion date September 2007
Est. primary completion date September 2007
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 75 Years
Eligibility Inclusion criteria:

- Thoracic surgery (thoracotomy, thoracoscopy) with one-lung ventilation

Exclusion criteria:

- Immunosuppressive therapy

- Ongoing inflammatory processes

Study Design

Allocation: Randomized, Endpoint Classification: Pharmacodynamics Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention


Related Conditions & MeSH terms

  • Thoracic Surgery With One-lung Ventilation

Intervention

Drug:
Sevoflurane/propofol
Sevoflurane/propofol

Locations

Country Name City State
Switzerland University Hospital of Zurich Zurich

Sponsors (1)

Lead Sponsor Collaborator
University of Zurich

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary One-lung ventilation measurement in the re-ventilated lung after short-period pulmonary collapse Sep 07 No