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N/A N=349 Randomized Single-blind Prevention

Walking and Dietary Modification for Recurrent Early Miscarriages

Recurrent Miscarriage

Enrolled (actual)
349
Serious AEs
0.0%
Results posted
Apr 2017
Primary outcome: Primary: Take-home Baby Rate — 152; 83 babies

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Walking & dietary modification (Behavioral)
Age
Adult · 18+ yrs
Sex
Female
Sponsor
Hospital dos Servidores do Estado do Rio de Janeiro
Primary completion
Aug 2016

Outcome Measures

OutcomeResultp-value
PRIMARY
Take-home Baby Rate
152; 83
SECONDARY
Gestational Diabetes Mellitus
4; 17
SECONDARY
Preeclampsia
8; 22
SECONDARY
Mothers Who Used Heparin for Nephrotic Range Proteinuria or Placental Insufficiency
10; 30
SECONDARY
Excessive Weight Gain
12; 21
SECONDARY
First-trimester Losses
21; 63
SECONDARY
Second and Third-trimester Losses
0; 7
SECONDARY
Live-born Children
153; 91
SECONDARY
Babies Born at Term
138; 57
SECONDARY
Appropriate-for-gestational Age Babies
141; 56
SECONDARY
Neonates With Hypoglycemia
3; 15

Summary

This study is part of a big one aiming to evaluate how lifestyle interventions during pregnancy affect obstetric results, neonatal metabolism and the intelligence of the offspring (study not yet completed). Data regarding obstetric and neonatal results were entered in NCT01409382, but we decided to split results in two for the sake of clarity. A cohort of women with early pregnancy losses without antiphospholipid antibodies was selected for two reasons. One is that these women follow strictly the recommendadtions. The second is that no medication has been shown to increase the rate of take-home babies in women with early miscarriages who test negative for antiphospholipid antibodies. We decided to focus on the fibrinolytic system because trophoblast migration and placental vasculogenesis and angiogenesis depend on plasmin-dependent extracellular matrix remodeling. Plasminogen activator inhibitor (PAI)-1 inhibits the generation of plasmin. Since both glucose and insulin increase PAI-1 synthesis, hyperglycemia itself, or by stimulating insulin production, reduces plasmin generation, which may impair placentation. Abnormalities in glucose metabolism may be also deleterious to embryos by causing epigenetic changes. Chromosomal abnormalities are considered an important cause of early pregnancy losses. Several lines of evidence lend support to the hypothesis that carbohydrate metabolism abnormalities contribute to the pathogenesis of recurrent early pregnancy losses. One is that of the pregnancies of the women with polycystic ovary syndrome, around 30 and 50% end with first-trimester miscarriages. Hyperinsulinemia is a prevalent feature of the syndrome, and interventions proven effective in reducing insulin levels, such as metformin, have been shown to reduce the rate of early miscarriages. The other is that patients with body mass index of ≥25 kg/m2 have significantly higher odds of early miscarriage, regardless of the method of conception. The investigator's hypothesis was that a balanced diet combined to regular exercise, by improving glucose homeostasis, would increase the take-home baby rate in women with consecutive early miscarriages. Moderate exercises are usually well tolerated not only by the mother, but also by the fetus, as indicated by tests of fetal well-being, including umbilical artery systolic to diastolic ratio.

Eligibility Criteria

Inclusion Criteria

  • ≥ 2 consecutive pregnancy losses in the first trimester;
  • losses should be documented by pathology or ultrasound-confirmed gestational sac.

Exclusion Criteria (any of the following):

  • anatomic anomalies that may increase the risk of pregnancy losses, not amenable to surgical correction during pregnancy, such as uterine septum;
  • antiphospholipid antibodies;
  • prior second- or third-trimester losses;
  • current multiple gestation;
  • disabilities such as hemiplegia or paraplegia;
  • renal or liver failure;
  • conditions requiring a priori anticoagulation
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03023137). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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