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Effect of Prophylatic Use of Enoxaparin in Women Undergoing in Vitro Fertilization Treatment

Effect of Prophylatic Use of Enoxaparin in Women Undergoing in Vitro Fertilization Treatment

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05225155
Enrollment
104
Registered
2022-02-04
Start date
2015-02-02
Completion date
2019-08-31
Last updated
2022-09-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Fertilization in Vitro, Infertility, Female, Thrombophilia

Keywords

female infertility, thrombophilia, enoxaparin, abortion, in vitro fertilization, low molecular weight heparin

Brief summary

Retrospective study designed to evaluate outcomes in patients undergoing assisted reproduction. Some of them had thrombophilia, and part of them was treated with enoxaparin, started on the day of embryo transfer, and the other part not. Women without thrombophilia formed the control group.

Detailed description

A retrospective study was performed to evaluate the results in 104 patients undergoing to assisted reproduction. Women without thrombophilia were included as controls (n=20), while women with thrombophilia were either treated with 40 mg daily of enoxaparin (treated group, n=54), initiated on the day of embryo transfer, and continued to the week 36 of gestation, or did not receive this medication (untreated group, n= 30).

Interventions

DRUGEnoxaparin

Women with thrombophilia were treated with 40 mg daily of enoxaparin (treated group), initiated on the day of embryo transfer, up to week 36 of gestation

Sponsors

Faculdade de Medicina do ABC
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
No

Inclusion criteria

* Women with female infertility or unexplained infertility * Normal sperm analysis

Exclusion criteria

* Women who did not agree with in vitro fertilization techniques

Design outcomes

Primary

MeasureTime frameDescription
Number of participants with detectable fetal heartbeatDay 28A transvaginal ultrasound was performed for detection of fetal heartbeat
Number of participants with detectable ongoing pregnancyWeek 12Ongoing pregnancy was detected by ultrasound at twelve weeks
Number of participants who delivered a live babyWeek 36Live birth was considered delivery that resulted in at least one live born neonate

Secondary

MeasureTime frameDescription
Number of participants with biochemical gestation detectedDay 14Serum beta-HCG detected 14 days after embryo transfer

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026