Risk Factors of Venous Thromboembolism After Incisional Ventral Hernia Repair.
1 other identifier
observational
240
1 country
1
Brief Summary
Aim of our study is to find frequency and risk factors for venous thromboembolism development in patients who underwent surgery for incisional ventral hernia. There were 240 patients enrolled in our retrospective observational cohort study. Included patients were operated for incisional hernia in Saveljev University Surgery Clinic from January 2018 to December 2019. Compression duplex ultrasound of lower legs veins was performed in 2-4 days after surgery for all participants. The primary endpoint was the occurrence of the venous thromboembolism event, including pulmonary embolism.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2018
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2019
CompletedStudy Completion
Last participant's last visit for all outcomes
January 31, 2020
CompletedFirst Submitted
Initial submission to the registry
May 23, 2022
CompletedFirst Posted
Study publicly available on registry
June 30, 2022
CompletedJune 30, 2022
June 1, 2022
2 years
May 23, 2022
June 27, 2022
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
venous thromboembolism
Screening ultrasound in the postoperative period was aimed at looking for signs of deep vein thrombosis. The imaged vessels included the common femoral, great saphenous, superficial femoral, deep femoral, popliteal, posterior tibial, and peroneal veins of both lower extremities. The presence of a thrombotic process in the vein was evidenced by the rigidity of its walls during compression by the sensor, the presence of hyperechoic inclusions, and the impossibility of visualizing blood flow during color mapping.
was performed with median 3 days (min 1 day, max 7 days, interquartile range 2-4 days) after surgery
Interventions
Open or laparoscopic hernia repair with mesh placement.
Eligibility Criteria
patients of Saveljev University Surgery Clinic, Moscow
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Pirogov Russian National Research Medical University
Moscow, 117997, Russia
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
May 23, 2022
First Posted
June 30, 2022
Study Start
January 1, 2018
Primary Completion
December 31, 2019
Study Completion
January 31, 2020
Last Updated
June 30, 2022
Record last verified: 2022-06