ClinicalTrials.gg
Status unknownNCT01971333Updated Oct 30, 2013

Dynamic Preload Parameters During Liver Transplantation

An observational study in Liver Cirrhosis, sponsored by National Taiwan University Hospital. Status unknown at 1 site in Taiwan. Open to participants aged 6 Months to 75 Years. Per ClinicalTrials.gov, last updated 2013-10-30.

Sponsored by National Taiwan University Hospital · Observational

The sponsor has not verified this record recently (last verified Oct 2013), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
80
Ages
6 Months to 75 Years
Sex
All
01

Study summary

The arterial system compliance is compromised in liver cirrhotic patients. Dynamic preload variables are either pressure-based (e.g.pulse pressure variation; PPV), flow-based (e.g. stroke volume variation; SVV), or volume-based (plethysmographic variability index; PVI). It is not yet clear that dynamic preload parameters based on which mechanism will be accurate to predict fluid responsiveness in the cirrhotic patients. Therefore, this study aimed to claried which dynamic preload parameters would be more accurate during the liver transplantation.

Read the detailed description

Fluid management is crucial during liver transplantation. Patients with cirrhosis and portal hypertension have an altered blood volume distribution and pooling in the splanchnic circulation. Excess administration of intravenous fluid may increase portal hypertension due to splanchnic venous congestion and may also aggravate coagulopathy by dilution. On the other hand, fluid restriction may risk systemic and especially renal hypoperfusion. Traditional static fluid parameter, such as central venous pressure, pulmonary artery occlusion pressure, have been reported inaccurate to predict fluid responsiveness. In comparison, the recent developed dynamic fluid parameters based on heart-lung interaction were reported to be good preload indicators in a variety of different surgical settings. However, the validity of such dynamic fluid parameters is highly dependent on The arterial system compliance is compromised in liver cirrhotic patients. Dynamic preload variables are either pressure-based (e.g.pulse pressure variation; PPV), flow-based (e.g. stroke volume variation; SVV), or volume-based (plethysmographic variability index; PVI). It is not yet clear that dynamic preload parameters based on which mechanism will be accurate to predict fluid responsiveness in the cirrhotic patients. Therefore, this study aimed to claried which dynamic preload parameters would be more accurate during the liver transplantation.

02

Conditions studied

  • Liver Cirrhosis

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Keywords

  • pulse pressure variation
  • stroke volume variation
  • plethysmographic variation index
  • fluid responsiveness
03

In context

Liver Cirrhosis

1,668 studies on the registry are indexed under Liver Cirrhosis; 360 are open to participants now.

This study's planned enrollment of 80 is below the median of 152 across 605 observational studies indexed under Liver Cirrhosis.

Browse Liver Cirrhosis studies →

Lead sponsor

National Taiwan University Hospital is the lead sponsor of 2,608 studies on the registry; 573 are open to participants now.

Of its 11 completed or terminated interventional studies of FDA-regulated products, 2 (18%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
6 Months to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

End stage liver disease patients scheduled for liver transplantation in National Taiwan University Hospital

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • End stage liver disease patients scheduled for liver transplantation in National Taiwan University Hospital

Exclusion criteria

Exclusion Criteria:

  • Allergic reaction
  • preexisting arrythmia
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
80 participants (estimated)
Patient registry
No

Groups and cohorts

  • Liver transplantation

    Compare intraoperative change of dynamic parameters after fluid loading: 1. pulse pressure variation 2. stroke volume variation 3. plethysmographic variation index

06

What researchers measure

Primary outcomes

  1. Change of cardiac index after fluid loading

    Time frame: one day

Secondary outcomes

  1. Fluid responsiveness parameters: pulse pressure variation

    Time frame: one day

  2. Fluid responsiveness parameters: stroke volume variation

    Time frame: one day

  3. Fluid responsiveness parameters: plethysmographic variation index

    Time frame: one day

Other outcomes

  1. Mean arterial pressure changes

    Time frame: one day

  2. Central venous pressure changes

    Time frame: one day

  3. Heart rate changes

    Time frame: one day

07

Study locations

1 of 1 sites recruiting
  • Department of Anesthesiology, NTUH, Taipei, Taiwan
    Taipei, Taiwan
    • Chun Yu Wu, M.D. · Contact · longersolo@gmail.com · +886-2-23123456
    • Chun Yu Wu, M.D. · Principal investigator
    Recruiting
08

References and documents

Publications

  • Vos JJ, Kalmar AF, Struys MM, Wietasch JK, Hendriks HG, Scheeren TW. Comparison of arterial pressure and plethysmographic waveform-based dynamic preload variables in assessing fluid responsiveness and dynamic arterial tone in patients undergoing major hepatic resection. Br J Anaesth. 2013 Jun;110(6):940-6. doi: 10.1093/bja/aes508. Epub 2013 Jan 24. PubMed 23348202 ↗
  • Wu CY, Cheng YJ, Liu YJ, Wu TT, Chien CT, Chan KC; NTUH Center of Microcirculation Medical Research (NCMMR). Predicting stroke volume and arterial pressure fluid responsiveness in liver cirrhosis patients using dynamic preload variables: A prospective study of diagnostic accuracy. Eur J Anaesthesiol. 2016 Sep;33(9):645-52. doi: 10.1097/EJA.0000000000000479. PubMed 27167058 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 30, 2013, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT01971333
Responsible party
Sponsor
First posted
Oct 29, 2013
Start date
Oct 2013
Primary completion
Oct 2014 (estimated)
Completion
Oct 2014 (estimated)
Last update
Oct 30, 2013

Study contacts

Chun Yu Wu, M.D.
Contact
longersolo@gmail.com
+886-2-23123456 ext. 62158
Chun Yu Wu, M.D.
principal investigator · Department of Anesthesiology, National Taiwan University Hospital

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Oct 2013. You cannot join it, but the record below documents what was studied.

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