Clinical Trials Directory

Trials / Completed

CompletedNCT02935530

Thromboprophylaxis After Surgery for Gynecologic Malignancy in China

Effectiveness and Safety of Thromboprophylaxis After Surgery for Gynecologic Malignancy in China

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
315 (actual)
Sponsor
Huazhong University of Science and Technology · Academic / Other
Sex
Female
Age
16 Years – 70 Years
Healthy volunteers
Not accepted

Summary

Venous thromboembolism (VTE) is an important cause of post-operative morbidity and mortality in women undergoing surgery for gynecologic malignancies. Although the benefit of thromboprophylaxis in reduction of post-operative VTE events after surgery for gynecologic cancers has been well documented around the world, the evidence for Chinese women is rare. The investigators designed this prospective and randomized study to assess the benefit of pharmacologic prophylaxis for patients received surgical treatment for gynecologic malignancies in China.

Conditions

Interventions

TypeNameDescription
DRUGs-LMWH2125KU, subcutaneous injection of 5-10 days
DRUGLMWH4250KU, subcutaneous injection of 5-10 days
DRUGArgatroban20mg, injection for 5-10 days

Timeline

Start date
2016-01-01
Primary completion
2017-08-01
Completion
2017-10-01
First posted
2016-10-17
Last updated
2019-05-14

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT02935530. Inclusion in this directory is not an endorsement.

Thromboprophylaxis After Surgery for Gynecologic Malignancy in China (NCT02935530) · Clinical Trials Directory