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CompletedNCT05058521Updated Sep 27, 2021

Venous thromboEmbolism Risk Profiles in Chinese hoSpitalized patiEnts (VERSE Study)

An observational study in Venous Thromboembolism, sponsored by Beijing Tsinghua Chang Gung Hospital. Completed at 1 site in China. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2021-09-27.

Sponsored by Beijing Tsinghua Chang Gung Hospital · Observational

Study type
Observational
Model
Other
Time perspective
Cross-sectional
Enrollment
27,490
Ages
18 Years and older
Sex
All
01

Study summary

Venous thromboembolism (VTE) is a complex multifactorial disease, mainly manifested by deep vein thrombosis (DVT) and pulmonary embolism (PE). VTE events increase the length of hospitalization and treatment costs and seriously affect the quality of life of patients, so it is increasingly appreciated to identify high-risk patients with VTE and take preventive measures. The Padua prediction score (PPS) and Caprini risk assessment model (RAM) are widely used in clinical practice as common risk assessment scales in medical and surgical departments, respectively. And D-dimer levels have been considered as a well indicator to rule out acute VTE. Previous epidemiological studies on VTE have found the risk of VTE is significantly higher in hospitalized patients than in the general population and the prophylaxis decisions vary among countries, hospitals and departments, indicating current in-hospital VTE prevention strategies are far from optimal and it's imperative to regionalized control of VTE. Therefore, a single-institution-based risk profile study of in-hospital VTE patients is designed to explore current situation of VTE occurrence and predictive efficacy of widely used risk assessment models as well as D-dimer in one of the general hospitals in Beijing, China.

Read the detailed description

In this study, the investigators recruited adult inpatients attending Tsinghua Chang Gung Hospital in Beijing from June 2018 to April 2020, screened for patients with a hospital stay over 3 days and new-onset of VTE during hospital stay, and identified the in-hospital VTE patients after excluding patients who presented for DVT and/or PE. Similarly, negative patients were selected by not having a VTE during hospital stay. The diagnosis of VTE was confirmed as the occurrence of a critical value alert during hospitalization, which was predefined as ultrasound/radiology report of DVT or/and PE. Data was collected from the TEACH database of Beijing Tsinghua Chang Gung Hospital affiliated with Tsinghua University.

Patients baseline characteristics were extracted from database. VTE risk assessment was conducted with either Caprini risk assessment model (surgical patients) or Padua prediction score (medical patients). The evaluation was started upon admission and regularly repeated depending on the patient's condition. The last evaluation was conducted before discharge. The D-dimer values during hospitalization were also collected.

The rate of in-hospital VTE, distributions of in-hospital VTE patients and the receiver operating characteristic curves were analyzed.

02

Conditions studied

  • Venous Thromboembolism

Keywords

  • VTE
  • China
  • Caprini risk assessment model
  • Padua prediction score
  • Risk profiles
03

In context

Thromboembolism

818 studies on the registry are indexed under Thromboembolism; 97 are open to participants now.

This study's enrollment of 27,490 is above the median of 500 across 344 observational studies indexed under Thromboembolism.

Browse Thromboembolism studies →

Lead sponsor

Beijing Tsinghua Chang Gung Hospital is the lead sponsor of 96 studies on the registry; 52 are open to participants now.

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

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

The investigators recruited adult inpatients attending Tsinghua Chang Gung Hospital in Beijing from June 2018 to April 2020.

Inclusion criteria

  1. Age 18 and over, male or female
  2. Inpatients with a hospital stay over 3 days
  3. With or without new-onset of VTE during their stay

Exclusion criteria

Exclusion Criteria:

  1. Patients who presented for DVT and/or PE
  2. Patients who were admitted in emergency department
05

Study design

Observational model
Other
Time perspective
Cross-sectional
Enrollment
27,490 participants (actual)
Target follow-up
23 Months
Patient registry
Yes

Groups and cohorts

  • In-hospital VTE group

    In-hospital VTE group includes patients who were with a hospital stay over 3 days and new-onset of VTE during their stay. Patients who presented for VTE were excluded.

  • Negative group

    Negative group includes patients who were with a hospital stay over 3 days and did not have a VTE during their hospital stay.

06

What researchers measure

Primary outcomes

  1. The rate of in-hospital VTE

    The diagnosis of VTE was confirmed as the occurrence of a critical value alert during hospitalization, which was predefined as ultrasound/radiology report of DVT or/and PE.

    Time frame: From June 2018 to April 2020

  2. Caprini risk assessment model scores

    Patients were stratified of VTE risk as very low risk (0), low risk (1-2), medium risk (3-4), high risk (5 and over).

    Time frame: Through discharge, an average of 20 days

  3. Padua prediction score scores

    Patients were stratified of VTE risk as low risk (0-3) and high risk (4 and over).

    Time frame: Through discharge, an average of 20 days

  4. D-dimer values

    The upper normal value 0.55mg/L FEU was used.

    Time frame: Through discharge, an average of 20 days

07

Study locations

1 site
  • Beijing Tsinghua Chang Gung Hosipital
    Beijing, 102218, China
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 27, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT05058521
Lead sponsor
Beijing Tsinghua Chang Gung Hospital
Responsible party
Sponsor
First posted
Sep 27, 2021
Start date
Jun 1, 2018
Primary completion
Apr 30, 2020
Completion
Apr 30, 2020
Last update
Sep 27, 2021

Study contacts

Weiwei Wu, MD
principal investigator · Beijing Tsinghua Chang Gung Hospital

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Sep 2021. You cannot join it, but the record below documents what was studied.

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