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Comparative Prevalence of Psychiatric Manifestations in Purely Obstetrical Antiphospholipid Syndrome (MENT-APL-O)

Primary Purpose

Antiphospholipid Syndrome

Status
Terminated
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Antiphospholipid antibody tests
Thrombophilia bloodwork
Psychiatric evaluation
Sponsored by
Centre Hospitalier Universitaire de Nīmes
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Antiphospholipid Syndrome focused on measuring Obstetrical antiphospholipid syndrome, Thrombophilia

Eligibility Criteria

18 Years - 45 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • The patient must have given his/her informed and signed consent
  • The patient must be insured or beneficiary of a health insurance plan
  • Not postmenopausal
  • Able to understand the nature, purpose and methodology of the study and agreed to cooperate in clinical and biological assessments
  • Available for 12 weeks of follow-up
  • Isolated obstetric morbidity, defined by at least one of the following criteria:
  • at least three consecutive episodes of unexplained, early, embryonic miscarriage, which occurred before the 10th week of pregnancy, with normal maternal anatomic and hormonal assessment, normal karyotypes for both biological parents;
  • at least one unexplained fetal death, defined as occurring after the 10th week of pregnancy, involving a morphologically normal fetus as documented by ultrasound examination or direct examination of the conceptus;
  • at least one premature birth of a morphologically normal fetus before the 34th week of pregnancy, because of: (1) pre-eclampsia, severe or not, according to the American College of Obstetrics and Gynecology, ACOG, 2002; (2)documented placental insufficiency, defined by the following parameters: (2a) abnormal or non-reassuring fetal monitoring exam, in general a non-reactive absence-of-fetal-stress test (fetal monitoring), suggesting fetal hypoxemia; (2b) a Doppler examination of uterine arteries suggesting fetal hypoxemia, ie the absence of end-diastolic flow in the umbilical arteries; (2c) oligohydramnios, that is to say, an amniotic flow index <5 cm; (2d) indexed birth weight for gestational age and sex below the 10th percentile.
  • Patient willing to accept psychological and medical care over the long term

Exclusion Criteria:

  • The patient is participating in another study
  • The patient is in an exclusion period determined by a previous study
  • The patient is under judicial protection, under tutorship or curatorship
  • The patient refuses to sign the consent
  • It is impossible to correctly inform the patient
  • The patient is pregnant, parturient or breastfeeding
  • Systemic vascular morbidity, defined by the following criteria: (1) Any personal history of venous thromboembolism, defined by the occurrence of deep phlebitis and / or a pulmonary embolism, diagnosed by means of objective exploration ; (2)Any personal history of superficial venous thrombosis; (3) Any personal history of clinical, symptomatic relapses of arterial insufficiency - the latter may be cerebro vascular in nature (transient ischemic attack, stroke, etc..), coronary in nature (angina, myocardial infarction, etc..) or otherwise (claudication mesenteric, etc.), and objectively diagnosed.
  • Systemic inflammatory disease: any history of systemic disease, lupus erythematosus or other connective, rheumatoid arthritis
  • Any history of neoplastic disease
  • Chronic antithrombotic treatment taken before the occurrence of obstetrical complications
  • Any chronic immunosuppressive therapy or immunomodulatory therapy (eg corticosteroids, hydroxochloroquine or intravenous immunoglobulins)
  • Fetal loss can be explained by infectious, metabolic (including rates of fasting blood glucose> 7 mmol / L), anatomical or hormonal factors
  • History of infection with hepatitis B, hepatitis C or HIV
  • Taking antipsychotic treatment potentially implicated in biological autoimmune abnormalities

Sites / Locations

  • APHM - Hôpital Nord
  • APHM - Hôpital de la Conception
  • APHM - Hôpital La Timone Adultes
  • CHU de Montpellier - Hôpital Saint-Eloi
  • CHU de Nîmes - Hôpital Universitaire Carémeau

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Other

Other

Other

Arm Label

Suspected Obstetrical APS; confirmed APS

Sus. Obst. APS, confirmed thrombophilia

Suspected Obstectrical APS; unconfirmed

Arm Description

The patients included in this study are women actively addressed to the participating departments because of clinical symptoms corresponding to suspected obstetrical anti-phospholipid syndrome. Bloodwork later confirms that these patients have APS. All patients included in this study will have the following interventions: antiphospholipid antibody tests thrombophilia bloodwork psychiatric evaluation

The patients included in this study are women actively addressed to the participating departments because of clinical symptoms corresponding to suspected obstetrical anti-phospholipid syndrome. Bloodwork later confirms that these patients are thrombophilic. All patients included in this study will have the following interventions: antiphospholipid antibody tests thrombophilia bloodwork psychiatric evaluation

The patients included in this study are women actively addressed to the participating departments because of clinical symptoms corresponding to suspected obstetrical anti-phospholipid syndrome. Bloodwork cannot confirm APS, nor thrombophilia. All patients included in this study will have the following interventions: antiphospholipid antibody tests thrombophilia bloodwork psychiatric evaluation

Outcomes

Primary Outcome Measures

presence/absence of (lifetime) psychiatric symptoms
The Mini International Neuropsychiatric Interview (MINI 6) will be used to determined the presence/absence of (lifetime) psychiatric symptoms.

Secondary Outcome Measures

presence/absence of (current) psychiatric symptoms
The Mini International Neuropsychiatric Interview (MINI 6) will be used to determined the presence/absence of (current) psychiatric symptoms.
SCID-1 score
Structured Clinical Interview for Disorders (SCID-1) score for patients with a positive MINI evaluation.
MDQ score
Mood Disorder Questionnaire score
BDI score
The Beck Depression Inventory (BDI) score for currently depressed patients only.
IDS-C score
Inventory of Depressive Symptomatology (IDS-C) for currently depressed patients.
presence/absence of lupus anticoagulant
presence/absence of anticardiolipid antibodies
presence/absence of anti-beta2-glycoprotein 1 antibodies
deficit in antithrombin: yes/no
Deficit in protein C: yes/no
Deficit in protein S: yes/no
Excess of FVIII: yes/no
Excess of coagulation factor VIII?
Excess of homocystein? yes/no
presence/absence of allele F5 1691A
F5 1691A: allele 1691A for the factor V leiden gene
presence/absence of allele F2 20210A
F2 20210A: allele 20210A for the prothrombin gene
presence/absence of allele JAK2 617F
JAK2 617F: 617f mutation at the jak2 gene
Age at beginning of psychiatric symptoms
in years
Age at beginning of APL or thrombophilia symptoms
in years

Full Information

First Posted
July 23, 2012
Last Updated
March 24, 2015
Sponsor
Centre Hospitalier Universitaire de Nīmes
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1. Study Identification

Unique Protocol Identification Number
NCT01649479
Brief Title
Comparative Prevalence of Psychiatric Manifestations in Purely Obstetrical Antiphospholipid Syndrome
Acronym
MENT-APL-O
Official Title
Comparative Prevalence of Psychiatric Manifestations in Purely Obstetrical Antiphospholipid Syndrome
Study Type
Interventional

2. Study Status

Record Verification Date
March 2015
Overall Recruitment Status
Terminated
Why Stopped
Impossible to include patients at a correct rate; patients don't want to come back so they refuse participation.
Study Start Date
April 2013 (undefined)
Primary Completion Date
September 2013 (Actual)
Study Completion Date
September 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre Hospitalier Universitaire de Nīmes

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The main objective of this study is to estimate the lifetime prevalence of major psychiatric disorders (axis I DSM-IV; Diagnostic and Statistical Manual of Mental Disorders, version IV) in a large sample of patients with developed clinical signs of pure obstetrical antiphospholipid syndrome (suspected APS).
Detailed Description
The secondary objectives of this study are: A. To compare the lifetime prevalence of these major disorders between groups; B. To assess the association of different, targeted, qualitative biomarkers with clinical symptomatology; C. To assess the association between the presence of "transitory APS" and the presence of psychiatric disorders; D. Estimate and compare the current prevalence (= the day of assessment) of major psychiatric disorders in the sample of patients who developed clinical signs of obstetrical APS; E. Estimate the current prevalence (= the day of assessment) and intensity of major depressive episodes (MDE) in the sample of patients; F. Compare the prevalence of current MDE and the intensity of depressive symptoms present between groups; G. Estimate and compare the (lifetime and current) prevalence by category of psychiatric disorders (psychotic, anxiety, mood, etc..) in the APS group with that in the thrombophilic group and the remaining group; H. To study the average age of onset of psychiatric disorders and clinical manifestations of APS in the sample of patients who developed clinical signs of obstetrical APS; I. Compare the mean ages between groups; J. Compare the mean age at onset of psychiatric disorders with the average age of the first clinical manifestation of the disease in the group of women with APS.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Antiphospholipid Syndrome
Keywords
Obstetrical antiphospholipid syndrome, Thrombophilia

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
Outcomes Assessor
Allocation
Non-Randomized
Enrollment
20 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Suspected Obstetrical APS; confirmed APS
Arm Type
Other
Arm Description
The patients included in this study are women actively addressed to the participating departments because of clinical symptoms corresponding to suspected obstetrical anti-phospholipid syndrome. Bloodwork later confirms that these patients have APS. All patients included in this study will have the following interventions: antiphospholipid antibody tests thrombophilia bloodwork psychiatric evaluation
Arm Title
Sus. Obst. APS, confirmed thrombophilia
Arm Type
Other
Arm Description
The patients included in this study are women actively addressed to the participating departments because of clinical symptoms corresponding to suspected obstetrical anti-phospholipid syndrome. Bloodwork later confirms that these patients are thrombophilic. All patients included in this study will have the following interventions: antiphospholipid antibody tests thrombophilia bloodwork psychiatric evaluation
Arm Title
Suspected Obstectrical APS; unconfirmed
Arm Type
Other
Arm Description
The patients included in this study are women actively addressed to the participating departments because of clinical symptoms corresponding to suspected obstetrical anti-phospholipid syndrome. Bloodwork cannot confirm APS, nor thrombophilia. All patients included in this study will have the following interventions: antiphospholipid antibody tests thrombophilia bloodwork psychiatric evaluation
Intervention Type
Biological
Intervention Name(s)
Antiphospholipid antibody tests
Intervention Description
Each patient will be tested for antiphospholipid antibodies.
Intervention Type
Biological
Intervention Name(s)
Thrombophilia bloodwork
Intervention Description
Bloodwork will be drawn up for: antithrombin, protein C, protein S Factor V Leiden polymorphisms (F5 1691A) prothrombin 20210A gene polymorphism (F2 20210A) JAK2 617F Mutation Homocysteine Factor VIII
Intervention Type
Other
Intervention Name(s)
Psychiatric evaluation
Intervention Description
During this consultation, the Mini International Neuropsychiatric Interview will be used to screen for psychiatric symptoms. Should the latter be detected, a further consult with a psychiatrist or a psychologist will be organized; this second consult will include the Mood Disorder Questionnaire (MDQ), the Beck Depression Inventory (BDI), the Inventory for Depressive Symptomatology - Clinician (IDS-C) and the Structured Clinical Interview for Disorders (SCID, DSM-IV).
Primary Outcome Measure Information:
Title
presence/absence of (lifetime) psychiatric symptoms
Description
The Mini International Neuropsychiatric Interview (MINI 6) will be used to determined the presence/absence of (lifetime) psychiatric symptoms.
Time Frame
baseline (transversal); Day 0
Secondary Outcome Measure Information:
Title
presence/absence of (current) psychiatric symptoms
Description
The Mini International Neuropsychiatric Interview (MINI 6) will be used to determined the presence/absence of (current) psychiatric symptoms.
Time Frame
baseline (transversal); Day 0
Title
SCID-1 score
Description
Structured Clinical Interview for Disorders (SCID-1) score for patients with a positive MINI evaluation.
Time Frame
baseline (transversal); Day 0 or up to Day 15
Title
MDQ score
Description
Mood Disorder Questionnaire score
Time Frame
baseline (transversal); Day 0
Title
BDI score
Description
The Beck Depression Inventory (BDI) score for currently depressed patients only.
Time Frame
baseline (transversal); Day 0 or up to Day 15
Title
IDS-C score
Description
Inventory of Depressive Symptomatology (IDS-C) for currently depressed patients.
Time Frame
baseline (transversal); Day 0 or up Day 15
Title
presence/absence of lupus anticoagulant
Time Frame
baseline (transversal); Day 0
Title
presence/absence of anticardiolipid antibodies
Time Frame
baseline (transversal); Day 0
Title
presence/absence of anti-beta2-glycoprotein 1 antibodies
Time Frame
baseline (transversal); Day 0
Title
deficit in antithrombin: yes/no
Time Frame
baseline (transversal); Day 0
Title
Deficit in protein C: yes/no
Time Frame
baseline (transversal); Day 0
Title
Deficit in protein S: yes/no
Time Frame
baseline (transversal); Day 0
Title
Excess of FVIII: yes/no
Description
Excess of coagulation factor VIII?
Time Frame
baseline (transversal); Day 0
Title
Excess of homocystein? yes/no
Time Frame
baseline (transversal); Day 0
Title
presence/absence of allele F5 1691A
Description
F5 1691A: allele 1691A for the factor V leiden gene
Time Frame
baseline (transversal); Day 0
Title
presence/absence of allele F2 20210A
Description
F2 20210A: allele 20210A for the prothrombin gene
Time Frame
baseline (transversal); Day 0
Title
presence/absence of allele JAK2 617F
Description
JAK2 617F: 617f mutation at the jak2 gene
Time Frame
baseline (transversal); Day 0
Title
Age at beginning of psychiatric symptoms
Description
in years
Time Frame
baseline (transversal); Day 0
Title
Age at beginning of APL or thrombophilia symptoms
Description
in years
Time Frame
baseline (transversal); Day 0

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: The patient must have given his/her informed and signed consent The patient must be insured or beneficiary of a health insurance plan Not postmenopausal Able to understand the nature, purpose and methodology of the study and agreed to cooperate in clinical and biological assessments Available for 12 weeks of follow-up Isolated obstetric morbidity, defined by at least one of the following criteria: at least three consecutive episodes of unexplained, early, embryonic miscarriage, which occurred before the 10th week of pregnancy, with normal maternal anatomic and hormonal assessment, normal karyotypes for both biological parents; at least one unexplained fetal death, defined as occurring after the 10th week of pregnancy, involving a morphologically normal fetus as documented by ultrasound examination or direct examination of the conceptus; at least one premature birth of a morphologically normal fetus before the 34th week of pregnancy, because of: (1) pre-eclampsia, severe or not, according to the American College of Obstetrics and Gynecology, ACOG, 2002; (2)documented placental insufficiency, defined by the following parameters: (2a) abnormal or non-reassuring fetal monitoring exam, in general a non-reactive absence-of-fetal-stress test (fetal monitoring), suggesting fetal hypoxemia; (2b) a Doppler examination of uterine arteries suggesting fetal hypoxemia, ie the absence of end-diastolic flow in the umbilical arteries; (2c) oligohydramnios, that is to say, an amniotic flow index <5 cm; (2d) indexed birth weight for gestational age and sex below the 10th percentile. Patient willing to accept psychological and medical care over the long term Exclusion Criteria: The patient is participating in another study The patient is in an exclusion period determined by a previous study The patient is under judicial protection, under tutorship or curatorship The patient refuses to sign the consent It is impossible to correctly inform the patient The patient is pregnant, parturient or breastfeeding Systemic vascular morbidity, defined by the following criteria: (1) Any personal history of venous thromboembolism, defined by the occurrence of deep phlebitis and / or a pulmonary embolism, diagnosed by means of objective exploration ; (2)Any personal history of superficial venous thrombosis; (3) Any personal history of clinical, symptomatic relapses of arterial insufficiency - the latter may be cerebro vascular in nature (transient ischemic attack, stroke, etc..), coronary in nature (angina, myocardial infarction, etc..) or otherwise (claudication mesenteric, etc.), and objectively diagnosed. Systemic inflammatory disease: any history of systemic disease, lupus erythematosus or other connective, rheumatoid arthritis Any history of neoplastic disease Chronic antithrombotic treatment taken before the occurrence of obstetrical complications Any chronic immunosuppressive therapy or immunomodulatory therapy (eg corticosteroids, hydroxochloroquine or intravenous immunoglobulins) Fetal loss can be explained by infectious, metabolic (including rates of fasting blood glucose> 7 mmol / L), anatomical or hormonal factors History of infection with hepatitis B, hepatitis C or HIV Taking antipsychotic treatment potentially implicated in biological autoimmune abnormalities
Facility Information:
Facility Name
APHM - Hôpital Nord
City
Marseille Cedex 20
ZIP/Postal Code
13915
Country
France
Facility Name
APHM - Hôpital de la Conception
City
Marseille Cedex 5
ZIP/Postal Code
13385
Country
France
Facility Name
APHM - Hôpital La Timone Adultes
City
Marseille cedex 5
ZIP/Postal Code
13385
Country
France
Facility Name
CHU de Montpellier - Hôpital Saint-Eloi
City
Montpellier
ZIP/Postal Code
34295
Country
France
Facility Name
CHU de Nîmes - Hôpital Universitaire Carémeau
City
Nîmes Cedex 09
ZIP/Postal Code
30029
Country
France

12. IPD Sharing Statement

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Comparative Prevalence of Psychiatric Manifestations in Purely Obstetrical Antiphospholipid Syndrome

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