search
Back to results

Low-molecular-weight Heparin (LMWH) Versus Unfractionated Heparin (UFH) in Pregnant Women With Recurrent Abortion Secondary to Antiphospholipid Syndrome

Primary Purpose

Recurrent Abortion

Status
Completed
Phase
Phase 2
Locations
Egypt
Study Type
Interventional
Intervention
enoxaparin 40mg plus low dose aspirin
Heparin calcium5,000 U twice daily plus low dose aspirin
Sponsored by
Cairo University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Recurrent Abortion focused on measuring Recurrent abortion, Antiphospholipid syndrome, unfractionated heparin, Low Molecular Weight Heparin

Eligibility Criteria

19 Years - 37 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients with a minimum of three consecutive pregnancy losses before 10 weeks gestation
  • Positive lupus anticoagulant and/or anticardiolipin antibodies (IgG and IgM) on at least two occasions twelve weeks apart .
  • Age between 19 - 37 years,
  • Body mass index between 19-30

Exclusion Criteria:

  • Parental chromosomal abnormalities
  • Uterine abnormalities
  • Luteal phase defect
  • Systemic lupus erythematosus
  • Previous thromboembolism
  • Sensitivity to aspirin.

Sites / Locations

  • Ahmed Elgazzar hospital
  • Cairo university hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

enoxaparin 40 mg plus low dose aspirin

Heparin calcium 5,000 U twice daily plus low dose aspirin

Arm Description

Outcomes

Primary Outcome Measures

Live Birth Rate = (Number of Live Births / Total Number of Pregnancies)
Live birth occurs when a fetus (> 24 weeks ) , exits the maternal body and subsequently shows signs of life, such as voluntary movement, heartbeat, or pulsation of the umbilical cord.

Secondary Outcome Measures

Minor and Major Bleeding
Thrombocytopenia
Preeclampsia
IUFD
Preterm Delivery
Spontaneous Osteoporotic Fractures

Full Information

First Posted
January 19, 2010
Last Updated
July 29, 2011
Sponsor
Cairo University
Collaborators
Ahmed Elgazzar Hospital
search

1. Study Identification

Unique Protocol Identification Number
NCT01051778
Brief Title
Low-molecular-weight Heparin (LMWH) Versus Unfractionated Heparin (UFH) in Pregnant Women With Recurrent Abortion Secondary to Antiphospholipid Syndrome
Official Title
Low-molecular-weight Heparin Versus Unfractionated Heparin in Pregnant Women With History of Recurrent Abortion Secondary to Antiphospholipid Syndrome. A Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
January 2010
Overall Recruitment Status
Completed
Study Start Date
June 2006 (undefined)
Primary Completion Date
November 2009 (Actual)
Study Completion Date
December 2009 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Cairo University
Collaborators
Ahmed Elgazzar Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The aim of this study is to compare the efficacy and safety of Low molecular weight heparin (LMWH) plus low dose aspirin (LDA) with unfractionated heparin(UFH) plus LDA in women with recurrent pregnancy loss associated with antiphospholipid syndrome (APS).
Detailed Description
Women with antiphospholipid syndrome (APS) have live birth rates as low as 10% in pregnancies without pharmacological treatment. Low dose aspirin (LDA) ,unfractionated heparin(UFH) , Low molecular weight heparin (LMWH) , prednisone, and intravenous immunoglobulin (IVIG) have been used either alone or in combination in order to improve the live birth rate in APS positive women with recurrent miscarriage. A Cochrane review of 13 randomized or quasi-randomized, controlled trials of various management options of pregnant women with a history of pregnancy loss and APL, revealed that combined UFH and aspirin was the treatment of choice which reduced pregnancy loss by 54% . During the past decade , low molecular weight heparins were widely used in the prophylaxis and treatment of patients with venous or arterial thrombosis ,with an efficacy and safety superior or at least equivalent to that of UFH .Although recent studies reported the use of LMWH in the management of patients recurrent pregnancy loss secondary to antiphospholipid syndrome resulted in encouraging results . It is not clear whether the efficacy and safety of LMWH is equivalent to that of UFH . Although LMWH is more expensive than UFH . LMWH has longer half life , greater bioavailability , more stable dose-response relationship than UFH and therefore can be administered once daily. Furthermore, LMWH requires less frequent monitoring than UFH and and has less adverse effect on bone mineral density and platelet count .These advantages make LMWH more attractive for the patients and physicians than UFH . There are only two studies which compared the efficacy of LMWH plus LDA with that of UFH plus LDA in the management of pregnant women with recurrent pregnancy loss secondary to APS. In addition ,no randomized controlled study has yet compared the efficacy of LMWH plus LDA with UFH plus LDA. The aim of this study is to compare the efficacy and safety of Low molecular weight heparin (LMWH) plus low dose aspirin (LDA) with unfractionated heparin(UFH) plus LDA in women with recurrent pregnancy loss associated with antiphospholipid syndrome (APS).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Recurrent Abortion
Keywords
Recurrent abortion, Antiphospholipid syndrome, unfractionated heparin, Low Molecular Weight Heparin

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
enoxaparin 40 mg plus low dose aspirin
Arm Type
Experimental
Arm Title
Heparin calcium 5,000 U twice daily plus low dose aspirin
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
enoxaparin 40mg plus low dose aspirin
Other Intervention Name(s)
Clexane 40 mg
Intervention Description
Enoxaparin 40mg/day by subcutaneous injection ( Clexane 40 mg, Aventis international, Sanofi-aventis France ) is started when the serum pregnancy test become positive. Enoxaparin is stopped 2 days before planned induction of labor or cesarean section and twice-daily unfractionated heparin (UFH) is initiated. The evening UFH dose is cancelled before planned caesarean section . The patients are asked to stop enoxaparin or UFH with the beginning of labor pains . Low dose aspirin (75 mg/day)(Aspocid Paediatric ,Chemical Industries Development (CID)) is started before conception and continued until 36 weeks gestation.
Intervention Type
Drug
Intervention Name(s)
Heparin calcium5,000 U twice daily plus low dose aspirin
Other Intervention Name(s)
Cal-Heparine
Intervention Description
Heparin Calcium 5,000 U twice daily (Cal-Heparine, Amoun Pharmaceutical Co, Egypt) by subcutaneous injection is started when the serum pregnancy test become positive. The evening UFH dose is cancelled before planned caesarean section . The patients are asked to stop UFH with the beginning of labor pains . Low dose aspirin (75 mg/day)(Aspocid Paediatric ,Chemical Industries Development (CID))is started before conception and continued until 36 weeks gestation .
Primary Outcome Measure Information:
Title
Live Birth Rate = (Number of Live Births / Total Number of Pregnancies)
Description
Live birth occurs when a fetus (> 24 weeks ) , exits the maternal body and subsequently shows signs of life, such as voluntary movement, heartbeat, or pulsation of the umbilical cord.
Time Frame
pregnancy > 24weeks gestation
Secondary Outcome Measure Information:
Title
Minor and Major Bleeding
Time Frame
Duration of pregnancy and puerperium
Title
Thrombocytopenia
Time Frame
Duration of pregnancy and puerperium
Title
Preeclampsia
Time Frame
Pregnancy > 20 weeks gestation
Title
IUFD
Time Frame
Pregnancy >24 weeks gestation
Title
Preterm Delivery
Time Frame
24 weeks gestation<Pregnancy <37weeks gestation
Title
Spontaneous Osteoporotic Fractures
Time Frame
Duration of pregnancy and puerperium

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
19 Years
Maximum Age & Unit of Time
37 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with a minimum of three consecutive pregnancy losses before 10 weeks gestation Positive lupus anticoagulant and/or anticardiolipin antibodies (IgG and IgM) on at least two occasions twelve weeks apart . Age between 19 - 37 years, Body mass index between 19-30 Exclusion Criteria: Parental chromosomal abnormalities Uterine abnormalities Luteal phase defect Systemic lupus erythematosus Previous thromboembolism Sensitivity to aspirin.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Usama M Fouda
Organizational Affiliation
Lecturer of obstetrics and Gynecology , Cairo university
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ahmed M Sayed
Organizational Affiliation
Assistant professor of obstetrics and Gynecology , Cairo university.
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ahmed Elgazzar hospital
City
Cairo
Country
Egypt
Facility Name
Cairo university hospital
City
Cairo
Country
Egypt

12. IPD Sharing Statement

Citations:
PubMed Identifier
15749498
Citation
Noble LS, Kutteh WH, Lashey N, Franklin RD, Herrada J. Antiphospholipid antibodies associated with recurrent pregnancy loss: prospective, multicenter, controlled pilot study comparing treatment with low-molecular-weight heparin versus unfractionated heparin. Fertil Steril. 2005 Mar;83(3):684-90. doi: 10.1016/j.fertnstert.2004.11.002.
Results Reference
background
PubMed Identifier
15307977
Citation
Stephenson MD, Ballem PJ, Tsang P, Purkiss S, Ensworth S, Houlihan E, Ensom MH. Treatment of antiphospholipid antibody syndrome (APS) in pregnancy: a randomized pilot trial comparing low molecular weight heparin to unfractionated heparin. J Obstet Gynaecol Can. 2004 Aug;26(8):729-34. doi: 10.1016/s1701-2163(16)30644-2.
Results Reference
background
PubMed Identifier
32358837
Citation
Hamulyak EN, Scheres LJ, Marijnen MC, Goddijn M, Middeldorp S. Aspirin or heparin or both for improving pregnancy outcomes in women with persistent antiphospholipid antibodies and recurrent pregnancy loss. Cochrane Database Syst Rev. 2020 May 2;5(5):CD012852. doi: 10.1002/14651858.CD012852.pub2.
Results Reference
derived
PubMed Identifier
21251653
Citation
Fouda UM, Sayed AM, Abdou AM, Ramadan DI, Fouda IM, Zaki MM. Enoxaparin versus unfractionated heparin in the management of recurrent abortion secondary to antiphospholipid syndrome. Int J Gynaecol Obstet. 2011 Mar;112(3):211-5. doi: 10.1016/j.ijgo.2010.09.010. Epub 2011 Jan 19.
Results Reference
derived

Learn more about this trial

Low-molecular-weight Heparin (LMWH) Versus Unfractionated Heparin (UFH) in Pregnant Women With Recurrent Abortion Secondary to Antiphospholipid Syndrome

We'll reach out to this number within 24 hrs