Perioperative Care of HVPG Measurement (CHESS1904): An International Multicenter Survey

Sponsor
Hepatopancreatobiliary Surgery Institute of Gansu Province (Other)
Overall Status
Recruiting
CT.gov ID
NCT04121520
Collaborator
LanZhou University (Other), Shandong Provincial Hospital (Other), Xingtai People's Hospital (Other), Zhejiang University (Other), Ankara University (Other), Chiba University Graduate School of Medicine (Other), Universitas Indonesia, Cipto Mangunkusumo National General Hospital (Other), S. Orsola-Malpighi Hospital, University of Bologna (Other), Universidade Federal de Pernambuco (Other), Hanyang University College of Medicine (Other)
200
10
21.5
20
0.9

Study Details

Study Description

Brief Summary

Hepatic venous pressure gradient (HVPG) is an invasive test and requires technical skills of the operator and specialized instruments. HVPG measurement and anesthesia can cause stress responses in the body, which in turn lead to inflammatory response and immune function suppression. Thus, the perioperative care for patients undergoing HVPG measurement is crucial. This research trial studies comprehensive patient and medical worker questionnaires in predicting complications in patients with cirrhosis undergoing HVPG measurement. Comprehensive patient and medical worker questionnaires may help identify complications, such as the need for assistance in taking medication, decreased mobility and released tension that may improve outcomes.

Condition or Disease Intervention/Treatment Phase
  • Other: Questionnaire

Detailed Description

Portal hypertension is an important factor affecting the clinical outcomes of cirrhosis patients, and its severity determines the occurrence of development of cirrhosis complications, such as rupture and bleeding of gastroesophageal varices, ascites, and hepatorenal syndrome. The direct measurement of portal pressure is an extremely invasive and high-risk procedure. In addition, changes in intra-abdominal pressure will affect the portal pressure, which leads to unreliable results. The hepatic venous pressure gradient (HVPG) is the difference between wedged hepatic venous pressure and free hepatic venous pressure and reflects the pressure difference between the hepatic portal vein and the intra-abdominal veins. In recent years, the status of HVPG in clinical application of cirrhotic portal hypertension has gradually improved. In 2016, the American Association for the Study of Liver Diseases (AASLD) issued a consensus on risk stratification, diagnosis, and management of portal hypertensive bleeding in cirrhosis and re-emphasized the value of HVPG in assessing the cirrhosis staging, occurrence of complications and treatment goals. However, HVPG is an invasive test and requires technical skills of the operator and specialized instruments. HVPG measurement and anesthesia can cause stress responses in the body, which in turn lead to inflammatory response and immune function suppression. Thus, the perioperative care for patients undergoing HVPG measurement is crucial. This research trial studies comprehensive patient and medical worker questionnaires in predicting complications in patients with cirrhosis undergoing HVPG measurement. Comprehensive patient and medical worker questionnaires may help identify complications, such as the need for assistance in taking medication, decreased mobility and released tension that may improve outcomes.

Study Design

Study Type:
Observational
Anticipated Enrollment :
200 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Perioperative Care of Hepatic Venous Pressure Gradient (HVPG) Measurement (CHESS1904): An International Multicenter Survey
Actual Study Start Date :
Oct 16, 2019
Anticipated Primary Completion Date :
Aug 1, 2021
Anticipated Study Completion Date :
Aug 1, 2021

Arms and Interventions

Arm Intervention/Treatment
Observational

At time of consent and within the same day of HVPG measurement, participants will be asked to complete a pre-operative assessment. Relevant statistics will be recorded during the HVPG procedure. Post-operative complication will also be collected and the satisfaction survey will be conducted.

Other: Questionnaire
Comprehensive perioperative assessment Questionnaire administration

Outcome Measures

Primary Outcome Measures

  1. Post-operative satisfaction [1 day]

    After the procedure of HVPG (within the same day), participants will be asked to complete a pain scale which was experienced during and after the HVPG procedure. The pain scale ranges from 0 to 10 with 0 representing 'not at all' and 10 representing 'excessively'.

Secondary Outcome Measures

  1. Pre-operative perception [1 day]

    At time of consent and within the same day of HVPG procedure, participants will be asked to complete a pain scale which was felt to be experienced during the HVPG procedure. The pain scale ranges from 0 to 10 with 0 representing 'not at all' and 10 representing 'excessively'.

  2. Number of intra-operative complications [1 day]

    Number of complications (e.g. vasovagal reflex, arrhymia, inadvertent arterial puncture, hypersensitivity to contrast agents, pneumothorax) happened during the HVPG procedure.

  3. Number of post-operative complications [1 day]

    Number of complications (e.g. bleeding at the puncture point, contrast-induced nephropathy, infection, jugular vein thrombosis) happened after the HVPG procedure.

  4. Methods selection of HVPG measurement [1 day]

    Including the selection of routes for insertion of catheter, hepatic vein used for the assessment and the angiographic catheter used during the HVPG procedure.

  5. The result of HVPG measurement [1 day]

    The mean value of HVPG measurements.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
Eligible participants must meet the following criteria:
  1. aged between 18-75 years, no restriction on gender;

  2. clinically and/or pathologically diagnosed sinusoidal cirrhosis;

  3. with written informed consent

  4. scheduled to undergo HVPG measurement according to the following indications: 1) assessment of the efficacy of primary and secondary prophylactic drugs for gastroesophageal variceal bleeding; 2) predicting the risk of gastroesophageal variceal bleeding and guiding the selection of the treatment regimens; 3) predicting of risk, progression, and clinical outcomes of decompensation events in cirrhosis; 4) evaluation of the efficacy of new drugs; 5) evaluation of the accuracy of new non-invasive techniques; diagnosis and differential diagnosis of types of portal hypertension.

Exclusion Criteria:
Those cases that meet any of the following criteria should be excluded:
  1. contradictions for HVPG measurement;

  2. pregnant or lactating woman;

  3. severe coagulopathy (international normalized ratio>5);

  4. severe heart, lung, or kidney disease.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Universidade Federal de Pernambuco Recife Brazil
2 The First Hospital of Lanzhou University Lanzhou Gansu China
3 Xingtai People's Hospital Xingtai Hebei China
4 Shandong Provincial Hospital affiliated to Shandong University Jinan Shandong China
5 The First Affiliated Hospital, School of Medicine, Zhejiang University Hangzhou Zhejiang China
6 Universitas Indonesia, Cipto Mangunkusumo National General Hospital Jakarta Indonesia
7 S. Orsola-Malpighi Hospital, University of Bologna Bologna Italy
8 Chiba University Graduate School of Medicine Chiba Japan
9 Hanyang University College of Medicine Seoul Korea, Republic of
10 Ankara University School of Medicine Ankara Turkey

Sponsors and Collaborators

  • Hepatopancreatobiliary Surgery Institute of Gansu Province
  • LanZhou University
  • Shandong Provincial Hospital
  • Xingtai People's Hospital
  • Zhejiang University
  • Ankara University
  • Chiba University Graduate School of Medicine
  • Universitas Indonesia, Cipto Mangunkusumo National General Hospital
  • S. Orsola-Malpighi Hospital, University of Bologna
  • Universidade Federal de Pernambuco
  • Hanyang University College of Medicine

Investigators

  • Principal Investigator: Xiaolong Qi, M.D., LanZhou University
  • Principal Investigator: Necati Örmeci, M.D., Ankara University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Xiaolong Qi, Director, Institute of Portal Hypertension, Hepatopancreatobiliary Surgery Institute of Gansu Province
ClinicalTrials.gov Identifier:
NCT04121520
Other Study ID Numbers:
  • CHESS1904
First Posted:
Oct 10, 2019
Last Update Posted:
Feb 24, 2021
Last Verified:
Feb 1, 2021
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 24, 2021