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Clinical Trials/NCT06528340
NCT06528340
Completed
Not Applicable

Study of Pregnancies Outcomes in Advanced Maternal Age Women

Centro di Ricerca Clinica Salentino1 site in 1 country1,000 target enrollmentJanuary 1, 2025

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Advanced Maternal Age Pregnancy
Sponsor
Centro di Ricerca Clinica Salentino
Enrollment
1000
Locations
1
Primary Endpoint
Pregnancy outcomes
Status
Completed
Last Updated
3 months ago

Overview

Brief Summary

Pregnancies occurring in advanced maternal age (AMA) have become more common over the last few decades for a variety of reasons. Prominent contributor to this trend are the significant advancement in assisted reproductive technology (ART) and the growing accessibility to egg donation. Delaying having children is generally associated with other variables, such as the availability of various forms of contraception, which have decreased the number of unintended births and given women more autonomy over when they choose to become pregnant. In addition, from a socioeconomic standpoint, greater education and career options for women are major contributors to this phenomenon. Women with postsecondary education are especially affected by this issue since they are more likely to miss out on professional opportunities, money, and social standing when they become mothers. Studies show that women with a tertiary level of education stay pregnant later in life, compared to women with a lower level of education. Moreover, severe economic volatility throughout the early adult years, delays in the establishment of partnerships and marriages, and the shift from family homes to independent living all serve to worsen the tendency. In this investigation, we will seek, with a critical eye, to evaluate the implications of a pregnant woman in AMA and her outcomes, trying to highlight all the possible complications and problems of a pregnancy in AMA, with an evaluation of a big volume of AMA women in pregnancy and at delivery.

Detailed Description

Aims: 1. Primary aim is to investigate outcomes of pregnancies in advanced maternal age, in relation to maternal morbidity 2. Secondary aim is to investigate neonatal outcomes of pregnancies in advanced maternal age 3. Third aim is to evaluate if the pregnancy outcomes differ in relation to conception (spontaneous, IVF/ET, IVF/DO/ET or CRYO) INCLUSION CRITERIA 1\. pregnants older than 45 yrs at the time of delivery, regardless mode of conception 2. gestational age ≥24 weeks of gestation EXCLUSION CRITERIA 1. missing data relevant for the study 2. surrogacy MATERIALS AND METHODS The study will be conducted as multicentric observational study including both vaginal and cesarean section deliveries in each participating center from January 1st 2019 until December 31st, 2025 (period of seven years). In each participating center, one person will be in charge for data collection and filling the SPSS database after obtaining the approval of the local Ethic Committee. As the study is observational and all the procedures will be conducted according to the local practice, informed consent from patients is not necessary. Following data collection and termination of the study, a single researcher will oversee the SPSS data collection for all the participating centers, checking the quality of data and submitting it for statistical analysis. The following data will be collected for each patient: 1. maternal age at delivery 2. gravidity 3. parity 4. gestational age at delivery 5. data about conception: spontaneous, IVF, oocyte donation 6. use of cryopreserved material 7. maternal comorbidity 8. maternal pregnancy complication 9. use of prenatal diagnostics 10. mode od delivery 11. neonatal weight and AS 12. presence of fetal anomalies 13. IUGR 14. placental pathology: previa, abruption, abnormally invasive placenta 15. peripartum hemorrhage 16. ICU treatment after delivery 17. duration of postpartum hospital treatment in days 18. prolonged postpartum hospitalization peripartum major complications (hysterectomy, hematoma, relaparotomy, ligation of major blood vessels (uterine, ovarian, iliac), etc.)

Registry
clinicaltrials.gov
Start Date
January 1, 2025
End Date
January 20, 2026
Last Updated
3 months ago
Study Type
Observational
Sex
Female

Investigators

Sponsor
Centro di Ricerca Clinica Salentino
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • pregnants older than 45 yrs at the time of delivery, regardless mode of conception
  • gestational age ≥24 weeks of gestation

Exclusion Criteria

  • missing data relevant for the study

Outcomes

Primary Outcomes

Pregnancy outcomes

Time Frame: 1 year

To investigate outcomes of pregnancies in advanced maternal age, in relation to maternal morbidity, as complications in pregnancy, gestational age at delivery, type of delivery, maternal pregnancy complications, placental pathology, peripartum hemorrages, duration of hospital stay, prolonged hospitalization, peripartum major complications, etc

Secondary Outcomes

  • Perinatal outcomes(1 year)

Study Sites (1)

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