Clinical Trials Directory

Trials / Completed

CompletedNCT02856295

anti10a Levels in Women Treated With LMWH in the Postpartum Period

anti10a Levels in Women Treated With LMWH in the Postpartum Period for Preventing Vein Thrombosis Events: A Comparison of Two Doses

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
136 (actual)
Sponsor
HaEmek Medical Center, Israel · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Accepted

Summary

The aim of this study is to compare between anti-10a levels in postpartum women receiving different prophylactic doses of LMWH: one group with LMWH doses adjusted by the women's weight and the second group receiving 1mg/kg to a maximum dose of 120 mg

Detailed description

pregnancy and postpartum period are associated with increased risk of thromboembolism. this risk is further increased in women with thrombophilia. This risk is higher in the postpartum period compared with pregnancy period, especially the risk for pulmonary embolism (PE). The American College Of Obstetrics and Gynecologists, The American college of chest physicians and The Royal College of obstetricians and gynecologists recommend using low molecular weight heparin during the postpartum period in women with thrombophilia and women with risk factor for developing thromboembolism. there is no specific guidelines regarding the best protocol based on the level of anti-10 a. This study will compare between two protocols based on anti-10a levels.

Conditions

Interventions

TypeNameDescription
DRUGclexane (LMWH)to compare tow doses of clexane for preventing VTE in postpartum women

Timeline

Start date
2021-11-20
Primary completion
2022-08-01
Completion
2022-08-01
First posted
2016-08-04
Last updated
2022-11-15

Locations

1 site across 1 country: Israel

Source: ClinicalTrials.gov record NCT02856295. Inclusion in this directory is not an endorsement.