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Serum Progesterone and Threatened Abortion During Lactation

P

Prof. Dr. Cemil Tascıoglu Education and Research Hospital Organization

Status

Not yet enrolling

Conditions

Threatened Abortion

Study type

Observational

Funder types

Other

Identifiers

NCT07357922
2025/517

Details and patient eligibility

About

This study aims to evaluate the effect of first-trimester maternal serum progesterone levels on threatened abortion in women who conceive during the lactation period. Serum progesterone concentrations will be measured in lactating pregnant women during the first trimester, and their association with the etiology of threatened abortion will be analyzed.

Threatened abortion is defined as vaginal bleeding occurring in the first trimester of pregnancy and represents a risk for early pregnancy loss. Previous studies have shown that serum progesterone levels may be lower in cases of threatened abortion compared to healthy pregnancies and play an essential role in predicting miscarriage risk. Serum progesterone is therefore considered a useful biomarker for assessing pregnancy viability and prognosis.

During lactation, progesterone levels may vary depending on breastfeeding duration and maternal hormonal status, and generally remain low, similar to follicular-phase levels in non-pregnant women. However, normal reference values during lactation are not well established. This study aims to contribute new data to the limited literature on the relationship between lactation, serum progesterone levels, and threatened abortion, and to provide insights that may help improve early pregnancy loss prevention strategies.

Full description

This study is designed to investigate the relationship between maternal serum progesterone levels and threatened abortion in women who conceive during the lactation period. The primary objective is to evaluate first-trimester serum progesterone concentrations in lactating pregnant women and to assess their role in the etiology and clinical course of threatened abortion.

Threatened abortion is characterized by vaginal bleeding during the first trimester of pregnancy and is associated with an increased risk of early pregnancy loss. Progesterone plays a critical role in the maintenance of early pregnancy by supporting endometrial receptivity, suppressing uterine contractility, and modulating maternal immune tolerance. Previous studies have demonstrated that serum progesterone levels tend to be lower in pregnancies complicated by threatened abortion compared to uncomplicated pregnancies, and that reduced progesterone concentrations may be predictive of subsequent miscarriage.

Lactation is associated with distinct hormonal changes, primarily mediated by elevated prolactin levels, which suppress ovulation and result in progesterone levels comparable to those observed during the follicular phase of the menstrual cycle. Although progesterone levels increase following conception, the hormonal milieu during lactation may influence progesterone production and regulation in early pregnancy. However, normal reference ranges for serum progesterone levels in lactating pregnant women have not been clearly established, and data regarding their association with threatened abortion remain limited.

In this study, pregnant women who conceive during the lactation period will be enrolled. Maternal serum progesterone levels will be measured during the first trimester, and participants will be evaluated for the presence or absence of threatened abortion, defined as first-trimester vaginal bleeding with a viable intrauterine pregnancy. Clinical, obstetric, and demographic data will be recorded to allow assessment of potential confounding factors.

By examining the relationship between serum progesterone levels and threatened abortion in lactating pregnancies, this study aims to provide new insights into the hormonal mechanisms underlying early pregnancy complications. The findings may contribute to improved risk stratification, early diagnosis, and management strategies for threatened abortion in this specific population. Additionally, the study seeks to expand the limited body of literature on lactation-associated hormonal changes during early pregnancy and their clinical implications.

Enrollment

150 estimated patients

Sex

Female

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Female participants aged 18 to 50 years.
  • Pregnant women who conceived during the lactation period.
  • Singleton pregnancy.
  • First-trimester pregnancy.
  • Availability of first-trimester serum progesterone measurement obtained as part of routine antenatal care.
  • Ongoing follow-up at the participating hospitals.

Exclusion criteria

  • Age under 18 years or over 50 years.
  • Multiple pregnancies.
  • Known chronic medical diseases.
  • Use of progesterone supplementation before serum progesterone measurement.
  • Missing or incomplete clinical or laboratory data.

Trial design

150 participants in 1 patient group

Lactating Pregnant Women (First Trimester)
Description:
Pregnant women who conceived during the lactation period and are in the first trimester of pregnancy. Maternal serum progesterone levels will be measured at enrollment. Participants will be prospectively followed to evaluate the occurrence of threatened abortion, defined as first-trimester vaginal bleeding with a viable intrauterine pregnancy. This is a prospective observational cohort study, and no interventions are assigned.

Trial contacts and locations

0

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Central trial contact

Burak D Aydoğdu, M.D.

Data sourced from clinicaltrials.gov

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