Prospective Study of BMD and Ca-P Metabolism in RSA Patients: LMWH Use Versus Control
Study Details
Study Description
Brief Summary
The goal of this prospective observational study is to learn about the effect of low molecular weight heparin (LMWH) application on bone mineral density (BMD) and on calcium-phosphorus metabolism in patients with recurrent spontaneous abortion (RSA), and to compare the degree of bone loss and changes in blood calcium and phosphorus in RSA patients and in control groups with normal pregnancy. By monitoring ultrasound BMD and serum indicators related to maternal bone formation and Ca-P metabolism, the association mechanism between long-term use of LMWH, maternal Ca-P regulation and bone loss will be constructed, so as to contribute to clinical treatment and lifestyle guidance during pregnancy in RSA patients.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Detailed Description
Women who meet the inclusion criteria at the outpatient clinic of Renji Hospital are recruited in this study from November 2022 to December 2023. Basic information of all subjects is recorded, including number of miscarriages, duration of breastfeeding, comorbidities, and intake of nutritional supplements. Subjects' medication use during the study is recorded as well. Subjects will undergo ultrasound BMD at six time points: before and after medication during pregnancy preparation, at 10, 24, 32 weeks of pregnancy, and at 42 days postpartum. Peripheral blood will also be collected at the time points above to measure serum osteocalcin, blood calcium, blood phosphorus, 25(OH) D, thyroid hormone, and parathyroid hormone levels. Subjects will be followed up to 42 days postpartum to observe pregnancy outcomes and health conditions of the newborn.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| LMWH group Continuous use of low molecular weight heparin for more than 3 months during pregnancy preparation and during pregnancy with a history of more than 2 consecutive miscarriages before 28 weeks of gestation |
Drug: Low molecular weight heparin
Continuous use of LMWH for more than 3 months during pregnancy preparation and through pregnancy
Other Names:
|
| control group No use of low molecular weight heparin during pregnancy preparation and throughout pregnancy and history of more than 2 consecutive miscarriages before 28 weeks of gestation |
Outcome Measures
Primary Outcome Measures
- ultrasound BMD before medication during pregnancy preparation [4 weeks]
use ultrasound to test heel bone mineral density before medication during pregnancy preparation
- ultrasound BMD after medication during pregnancy preparation [up to 16 weeks]
use ultrasound to test heel bone mineral density after medication during pregnancy preparation
- ultrasound BMD at 10th weeks of pregnancy [up to 26 weeks]
use ultrasound to test heel bone mineral density at 10th weeks of pregnancy
- ultrasound BMD at 24th weeks of pregnancy [40 weeks]
use ultrasound to test heel bone mineral density at 24th weeks of pregnancy
- ultrasound BMD at 32nd weeks of pregnancy [1 year]
use ultrasound to test heel bone mineral density at 32nd weeks of pregnancy
- ultrasound BMD at postpartum [up to 1 year and 2 months]
use ultrasound to test heel bone mineral density at postpartum
Secondary Outcome Measures
- osteocalcin before medication during pregnancy preparation [4 weeks]
use peripheral blood test to detect N-terminal mid-molecular fragment of serum osteocalcin before medication during pregnancy preparation
- osteocalcin after medication during pregnancy preparation [up to 16 weeks]
use peripheral blood test to detect N-terminal mid-molecular fragment of serum osteocalcin after medication during pregnancy preparation
- osteocalcin at 10th weeks of pregnancy [up to 26 weeks]
use peripheral blood test to detect N-terminal mid-molecular fragment of serum osteocalcin at 10th weeks of pregnancy
- osteocalcin at 24th weeks of pregnancy [40 weeks]
use peripheral blood test to detect N-terminal mid-molecular fragment of serum osteocalcin at 24th weeks of pregnancy
- osteocalcin at 32nd weeks of pregnancy [1 year]
use peripheral blood test to detect N-terminal mid-molecular fragment of serum osteocalcin at 32nd weeks of pregnancy
- osteocalcin at postpartum [up to 1 year and 2 months]
use peripheral blood test to detect N-terminal mid-molecular fragment of serum osteocalcin at postpartum
- calcium before medication during pregnancy preparation [4 weeks]
use peripheral blood test to detect calcium level before medication during pregnancy preparation
- calcium after medication during pregnancy preparation [up to 16 weeks]
use peripheral blood test to detect calcium level after medication during pregnancy preparation
- calcium at 10th weeks of pregnancy [up to 26 weeks]
use peripheral blood test to detect calcium level at 10th weeks of pregnancy
- calcium at 24th weeks of pregnancy [40 weeks]
use peripheral blood test to detect calcium level at 24th weeks of pregnancy
- calcium at 32nd weeks of pregnancy [1 year]
use peripheral blood test to detect calcium level at 32nd weeks of pregnancy
- calcium at postpartum [up to 1 year and 2 months]
use peripheral blood test to detect calcium level at postpartum
- PTH before medication during pregnancy preparation [4 weeks]
use peripheral blood test to detect parathyroid hormone level before medication during pregnancy preparation
- PTH after medication during pregnancy preparation [up to 16 weeks]
use peripheral blood test to detect parathyroid hormone level after medication during pregnancy preparation
- PTH at 10th weeks of pregnancy [up to 26 weeks]
use peripheral blood test to detect parathyroid hormone level at 10th weeks of pregnancy
- PTH at 24th weeks of pregnancy [40 weeks]
use peripheral blood test to detect parathyroid hormone level at 24th weeks of pregnancy
- PTH at 32nd weeks of pregnancy [1 year]
use peripheral blood test to detect parathyroid hormone level at 32nd weeks of pregnancy
- PTH at postpartum [up to 1 year and 2 months]
use peripheral blood test to detect parathyroid hormone level at postpartum
- live bitrh [1 year]
A live baby born after 23 weeks of gestation
Eligibility Criteria
Criteria
Inclusion Criteria:
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Age between 18 to 45 years.
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Female who needs to prepare for pregnancy or have a confirmed pregnancy
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normal karyotype of chromosomes.
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normal uterine anatomy under pelvic ultrasound examination.
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Cooperation in completing blood sample collection, testing and ultrasound examination.
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no serious medical or surgical comorbidities.
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Sign the informed consent form.
Exclusion Criteria:
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Presence of diseases affecting calcium metabolism, including primary hyperparathyroidism, Cushing's disease, chronic liver, kidney and gastrointestinal (e.g., celiac disease) disorders and rheumatoid arthritis.
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Known HIV positive and / or screening visit, HBsAg or HCV antibody positive.
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The malignant tumors occurred in the past 5 years (except for the skin squamous basal cell carcinoma which has been resected and considered cured). Subjects who developed malignancies five years ago should provide evidence of remission or cure. Subjects with a history of cervical cancer who had undergone conization or cure in the past 3 years were eligible.
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Patients with a history of chronic infection such as Mycoplasma, chlamydia, Cryptococcus and invasive fungal infection should be discussed with the main researchers.
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History of active tuberculosis (TB) or evidence of previous TB infection. Subjects with a history of potential TB infection should also be excluded, unless there is a documented evidence that they have completed appropriate anti TB treatment in accordance with CDC guidelines or local regulations before screening. In addition, subjects were strictly forbidden to have any clinical symptoms / signs of active TB.
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Presence of pregnancy contraindications.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Renji Hospital, Shanghai Jiaotong University School of Medicine | Shanghai | Shanghai | China | 200127 |
Sponsors and Collaborators
- Aimin Zhao
Investigators
- Principal Investigator: Aimin Zhao, MD, Renji Hospital Affiliated to Shanghai Jiao Tong University School of Medicine
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- IIT-2023-0010