Hydroxychloroquine for Prevention of Recurrent Miscarriage. (BBQ)
Primary Purpose
Recurrent Miscarriage, First Trimester Abortion
Status
Active
Phase
Phase 3
Locations
France
Study Type
Interventional
Intervention
Hydroxychloroquine
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Recurrent Miscarriage focused on measuring Unexplained Recurrent Miscarriage, First trimester abortion, Hydroxychloroquine, Antiphospholipid antibody
Eligibility Criteria
Inclusion Criteria:
- women aged from 18 to 38 years,
- women trying to conceive,
- women with at least 3 previous consecutive miscarriage in the first pregnancy trimester, of unknown origin (normal parental karyotypes, no uterine cavity abnormality, no antiphospholipid syndrome with other clinical events than RM in the first trimester of pregnancy.)
- women who have given their informed consent
Exclusion Criteria:
- ongoing pregnancy,
- Normal pregnancy since the last miscarriage,
- Uterine cavity abnormality,
- Abnormal parental karyotype,
- Antiphospholipid syndrome defined as both persistent positive antiphospholipid antibodies (40 IU or more of anticardiolipin or anti beta2 GPI IgG or IgM, and/or lupus anticoagulant) and a specific clinical setting (thrombotic or obstetrical, apart from RM)
- women with a contraindication or an indication to a treatment by hydroxychloroquine
- Previous exposure > 4 years to chloroquine or hydroxychloroquine
- impossible follow up
Sites / Locations
- Centre Hospitalier Annecy Genevois
- CH d'Auch
- CHU Besançon
- CHRU de Brest
- CHU Estaing
- CHRU de Lille
- Hôpital Nord - Unité mère-enfant
- CH de Mont de Marsan
- CHU de Nantes
- Hopital Port Royal Cochin
- Hopital Saint Antoine
- Hôpital Bichat
- CHG François Mitterand
- Centre hospitalier de Cornouaille
- Hôpital sud de Rennes
- CHU de Saint Etienne - Hôpital Nord
- Nouvel Hôpital Civil
- CH de Bigorre
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Hydroxychloroquine
Placebo
Arm Description
The treatment will be orally administrated, at a daily dose of 400 mg of hydroxychloroquine . The treatment will be started before conception and will be stopped at the end of the tenth week of gestation or before in case of pregnancy loss.
A similar placebo will be orally administrated every day.
Outcomes
Primary Outcome Measures
A live and viable birth
In case of preterm and/or low birth weight, we define the viability by the decision to transfer the newborn to a neonatal intensive care unit
Secondary Outcome Measures
a live and viable birth (for the subgroup analyses)
occurrence of pregnancy complications (Recurrent Miscarriage-any other premature termination of pregnancy-placental vascular disease)
gestation time (in weeks of amenorrhea) at delivery,
birth weight (in grams) at delivery
survival of the newborn
psychomotor development of the child (normal/abnormal)
psychomotor development of the child (normal/abnormal)
height (in centimeters)
height (in centimeters)
weight (in grams)
weight (in grams)
Cranial perimeter (in centimeters)
Cranial perimeter (in centimeters)
Full Information
NCT ID
NCT03165136
First Posted
May 3, 2017
Last Updated
September 29, 2023
Sponsor
University Hospital, Brest
1. Study Identification
Unique Protocol Identification Number
NCT03165136
Brief Title
Hydroxychloroquine for Prevention of Recurrent Miscarriage.
Acronym
BBQ
Official Title
Prévention Des Fausses Couches Spontanées Répétées Par Hydroxychloroquine. Essai thérapeutique Multicentrique, randomisé, en Double Insu, Contre Placebo
Study Type
Interventional
2. Study Status
Record Verification Date
September 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
December 4, 2017 (Actual)
Primary Completion Date
November 1, 2025 (Anticipated)
Study Completion Date
February 1, 2026 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Brest
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Recurrent miscarriage (RM) defined by >=3 consecutive losses affects 1% of fertile couples. Most women have recurrent early loss with a failure of development before 10 weeks' gestation. Standard investigations fail to reveal any apparent cause in >50% of couples.
No study has demonstrated any benefit of any medication in women with Unexplained RM, in the presence or absence of an inherited thrombophilia.
Moreover, the benefit of aspirin and/or heparin has not been proved in women with Antiphospholipid (APL) antibody without other clinical manifestations of Antiphospholipid Syndrome.
Hydroxychloroquine (HQ) is a molecule whose properties (anti-thrombotic, vascular-protective, immunomodulatory, improved glucose tolerance, lipid-lowering, anti-infectious) could be useful against mechanisms of Unexplained RM.
There is no data concerning the benefit of HQ in RM in the presence or absence of antiphospholipid antibodies or any inherited thrombophilia.
Administration in (Systemic Lupus erythematosus (SLE) women and for Malaria prevention provides extensive safety data during pregnancy.
Oral administration makes possible treatment since the preconception period. For all of that and its low cost, hydroxychloroquine should be evaluated in RM whatever the woman thrombophilic status.
Detailed Description
Regarding the mechanisms of unexplained RM, on the basis of animal models and clinical studies, many hypotheses were raised:
Reduced ovarian reserve,
Progesterone defect: a double-blind trial did not show any benefit of progesterone therapy.
Thrombotic mechanisms and/or endothelial dysfunction: An association with some inherited thrombophilias was suggested. A prothrombotic state outside of pregnancy was measured in women with previous RM and without known thrombophilia.
Immunological disturbances (high titers of anti-thyroid or APL antibodies, maternal carriage of specific HLA alleles and immunological reactions against male-specific minor antigens, increased numbers of peripheral blood natural killer, overexpression of TOLL receptors, increase of TH1 and TH17 processes). Consequently, immunomodulatory treatments were proposed and assessed (no impact of intravenous immunoglobulins and no conclusive benefit of corticosteroids).
Miscellaneous: BMI> 30 and chronic endometritis. Besides, the experience gained from previous clinical trials in RM leads us to emphasize, that subcutaneous administration of heparin limits its assessment among fertile women. Indeed, the treatment could not be administrated before conception and consequently the exposure was often too short (injections cannot be routinely initiated before 5 weeks).
Except psychological support, there is no treatment whose benefit has been proved in unexplained RM, in the presence or in the absence of an inherited thrombophilia. Moreover the absence of benefit of some treatments has been clearly demonstrated. Although the prognostic is not so poor (live-birth rates around 70%), proposed therapeutic interventions are sometimes excessive (regarding possible side effects and cost): as intravenous immunoglobulins, assisted procreation ...anti-TNF.
Consequently, for the management of these distressed patients, investigating other therapeutic options is highly needed.
Regarding recurrent miscarriage in women with high titers of antiphospholipid but without any other previous clinical event listed in the antiphospholipid syndrome, the benefit of antithrombotic treatment remains controversial (negative results of the HepASA trial) and hydroxychloroquine has never been assessed, although retrospective studies are encouraging.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Recurrent Miscarriage, First Trimester Abortion
Keywords
Unexplained Recurrent Miscarriage, First trimester abortion, Hydroxychloroquine, Antiphospholipid antibody
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Model Description
Double Blind Randomized clinical trial
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
Active drug and placebo will be exactly the same
Allocation
Randomized
Enrollment
300 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Hydroxychloroquine
Arm Type
Experimental
Arm Description
The treatment will be orally administrated, at a daily dose of 400 mg of hydroxychloroquine . The treatment will be started before conception and will be stopped at the end of the tenth week of gestation or before in case of pregnancy loss.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
A similar placebo will be orally administrated every day.
Intervention Type
Drug
Intervention Name(s)
Hydroxychloroquine
Intervention Description
Hydroxychloroquine : 200 mg twice a day
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
placebo of hydroxychloroquine
Primary Outcome Measure Information:
Title
A live and viable birth
Description
In case of preterm and/or low birth weight, we define the viability by the decision to transfer the newborn to a neonatal intensive care unit
Time Frame
At delivery
Secondary Outcome Measure Information:
Title
a live and viable birth (for the subgroup analyses)
Time Frame
At delivery
Title
occurrence of pregnancy complications (Recurrent Miscarriage-any other premature termination of pregnancy-placental vascular disease)
Time Frame
Since the beginning of pregnancy up to delivery
Title
gestation time (in weeks of amenorrhea) at delivery,
Time Frame
At delivery up
Title
birth weight (in grams) at delivery
Time Frame
At delivery
Title
survival of the newborn
Time Frame
At 28 days of the newborn
Title
psychomotor development of the child (normal/abnormal)
Time Frame
at 6 months of age
Title
psychomotor development of the child (normal/abnormal)
Time Frame
at 12 months of age
Title
height (in centimeters)
Time Frame
at 6 months of age
Title
height (in centimeters)
Time Frame
at 12 months of age
Title
weight (in grams)
Time Frame
at 6 months of age
Title
weight (in grams)
Time Frame
at 12 months of age
Title
Cranial perimeter (in centimeters)
Time Frame
at 6 months of age
Title
Cranial perimeter (in centimeters)
Time Frame
at 12 months of age
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
38 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
women aged from 18 to 38 years,
women trying to conceive,
women with at least 3 previous consecutive miscarriage in the first pregnancy trimester, of unknown origin (normal parental karyotypes, no uterine cavity abnormality, no antiphospholipid syndrome with other clinical events than RM in the first trimester of pregnancy.)
women who have given their informed consent
Exclusion Criteria:
ongoing pregnancy,
Normal pregnancy since the last miscarriage,
Uterine cavity abnormality,
Abnormal parental karyotype,
Antiphospholipid syndrome defined as both persistent positive antiphospholipid antibodies (40 IU or more of anticardiolipin or anti beta2 GPI IgG or IgM, and/or lupus anticoagulant) and a specific clinical setting (thrombotic or obstetrical, apart from RM)
women with a contraindication or an indication to a treatment by hydroxychloroquine
Previous exposure > 4 years to chloroquine or hydroxychloroquine
impossible follow up
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Elisabeth PASQUIER, MD
Organizational Affiliation
EA3878 - University Hospital of Brest
Official's Role
Principal Investigator
Facility Information:
Facility Name
Centre Hospitalier Annecy Genevois
City
Annecy
ZIP/Postal Code
74374
Country
France
Facility Name
CH d'Auch
City
Auch
ZIP/Postal Code
32008
Country
France
Facility Name
CHU Besançon
City
Besançon
ZIP/Postal Code
25030
Country
France
Facility Name
CHRU de Brest
City
Brest
ZIP/Postal Code
29609
Country
France
Facility Name
CHU Estaing
City
Clermont-Ferrand
Country
France
Facility Name
CHRU de Lille
City
Lille
ZIP/Postal Code
59037
Country
France
Facility Name
Hôpital Nord - Unité mère-enfant
City
Marseille
ZIP/Postal Code
13015
Country
France
Facility Name
CH de Mont de Marsan
City
Mont-de-Marsan
ZIP/Postal Code
40000
Country
France
Facility Name
CHU de Nantes
City
Nantes
ZIP/Postal Code
44093
Country
France
Facility Name
Hopital Port Royal Cochin
City
Paris 14
ZIP/Postal Code
75679
Country
France
Facility Name
Hopital Saint Antoine
City
Paris
ZIP/Postal Code
75012
Country
France
Facility Name
Hôpital Bichat
City
Paris
ZIP/Postal Code
75018
Country
France
Facility Name
CHG François Mitterand
City
Pau
ZIP/Postal Code
64 000
Country
France
Facility Name
Centre hospitalier de Cornouaille
City
Quimper
ZIP/Postal Code
29000
Country
France
Facility Name
Hôpital sud de Rennes
City
Rennes
ZIP/Postal Code
35200
Country
France
Facility Name
CHU de Saint Etienne - Hôpital Nord
City
Saint Etienne
ZIP/Postal Code
42 270
Country
France
Facility Name
Nouvel Hôpital Civil
City
Strasbourg
ZIP/Postal Code
67091
Country
France
Facility Name
CH de Bigorre
City
Tarbes
ZIP/Postal Code
65013
Country
France
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
30898821
Citation
Pasquier E, de Saint-Martin L, Marhic G, Chauleur C, Bohec C, Bretelle F, Lejeune-Saada V, Hannigsberg J, Plu-Bureau G, Cogulet V, Merviel P, Mottier D. Hydroxychloroquine for prevention of recurrent miscarriage: study protocol for a multicentre randomised placebo-controlled trial BBQ study. BMJ Open. 2019 Mar 20;9(3):e025649. doi: 10.1136/bmjopen-2018-025649.
Results Reference
derived
Learn more about this trial
Hydroxychloroquine for Prevention of Recurrent Miscarriage.
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