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Completed

NCT Number: NCT01886664

Comparison of PRS According to Inhalation Agent During LDLT

The investigators tried to evaluate the effect of desflurane on the incidence of postreperfusion syndrome during living donor liver transplantation surgery. The investigators used sevoflurane as a comparison.

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Key information

Conditions

Liver Transplantation Postreperfusion Syndrome

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Seoul National University Hospital

Seoul, 110-744, South Korea

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • elective LDLT

Exclusion criteria

  • age < 18, age > 65
  • patient refusal
  • re-transplantation

Treatment and study plan

Sevoflurane

Drug

Desflurane

Drug

Primary outcomes

  1. frequency of PRS

    Time frame: immediately after reperfusion

    reperfusion syndrome occurs, if it occurs, immediately after reperfusion. Therefore, the primary outcome, reperfusion syndrome, can only be assessed immediately after reperfusion.

Secondary outcomes

  1. ICU length of stay

    Time frame: after LT until the patient is transferred to the ward

Sponsors and collaborators

Lead sponsor

Seoul National University Hospital

Other

Registry information

Important dates

Study start
2012
Primary completion
2013
Study completion
2013
First posted
Jun 26, 2013
Registry last updated
Jun 26, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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