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Not yet recruitingNCT05872009GaPUpdated May 23, 2023

Gestational Diabetes Mellitus: "Placental-maternal Crosstalk and Future Health"

An observational study in Gestational Diabetes, Cardiovascular Diseases and Placenta Diseases, sponsored by Oslo University Hospital. Not yet recruiting at 1 site in Norway. Open to female participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2023-05-23.

Sponsored by Oslo University Hospital · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
350
Ages
18 Years and older
Sex
Female
01

Study summary

The GaP study is designed to close important knowledge gaps by:

  1. exploring placental health and cellular ageing in GDM and the association with neonatal outcome
  2. evaluating the effectiveness of current and novel maternal health follow-up strategies after GDM
Read the detailed description

The incidence of gestational diabetes mellitus (GDM) is increasing. GDM has potential adverse short and long term health effects for both the women and her offspring, and involves dysfunctional interaction between placenta and the maternal body. The burden for the individual, the health system and society warrants further investigations into the placental-maternal crosstalk in GDM in order to improve personalized pregnancy surveillance and follow-up. In Oslo county, nearly twice as many women who give birth suffer from GDM (5.7%) than from preeclampsia (2.3%). The large obstetric department at Ullevål provides an optimal environment for novel translational studies and clinical practical aspects of GDM. The GaP study is designed to close important knowledge gaps by:

  1. exploring placental health and cellular ageing in GDM and the association with neonatal outcome
  2. evaluating the effectiveness of current and novel maternal health follow-up strategies after GDM
02

Conditions studied

  • Gestational Diabetes
  • Cardiovascular Diseases
  • Placenta Diseases
03

Who can participate

Ages eligible
18 Years and older
Sexes eligible
Female
Sampling method
Non-probability sample

Study population

Pregnant women with GDM (diagnosed according to guidelines and referred to our outpatient clinic) and healthy, euglycemic pregnant women (Control group: referred for breech evaluation, planning of elective cesarean section, suspected reduced or increased fetal growth with a normal finding at ultrasound). Patients can be recruited from outpatient clinic, prior to induction, at admission for elective cesaerean section or at admission for labor (but not yet in active labor)

Inclusion criteria

  • Pregnant women >18 years with GDM giving birth at Oslo University hospital Ullevål.
  • Control group of gestational age matched euglycemic, normotensive pregnancies

Exclusion criteria

Exclusion Criteria:

  • reduced fetal movements,
  • epilepsy
  • thyroidea dysfunction
  • hypertensive disorder of pregnancy
  • non-communicable disease
  • Communicable disease (such as HIV)
  • type 1 or type 2 diabetes.
  • not able to understand Norwegian or English.
  • under legal guardianship.
04

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
350 participants (estimated)
Patient registry
No
Biospecimen retention
Samples with dna

Groups and cohorts

  • Women with gestational diabetes

    Any treatment. N=200.

  • Control group

    Gestational-age matched, euglycemic, normotensive pregnant women (n=150)

05

What researchers measure

Primary outcomes

  1. Number of women with altered levels of circulating senescence markers

    Levels of maternal circulating senescence markers, e.g. SAA1, free thiol and related markers, in case group compared to controls

    Time frame: 4 years

  2. Number of women with altered levels of tissue-based senescence markers

    Expression of markers of senescence in placental tissue, as assesed by immunohistochemistry (e.g. IL-6, p21, p16 and related markers) in case group compared to controls

    Time frame: 4 years

  3. Number of women with increased values for postpartum surrogate markers for impaired cardiovascular function

    As assessed by circulating maternal levels of cardiovascular biomarkers, e.g. HDL (mmol/l), LDL (mmol/l) and related markers in case group compared to controls

    Time frame: 4 years

  4. Number of women with increased values for postpartum surrogate markers for impaired cardiovascular function

    As assessed by circulating maternal levels of cardiovascular biomarkers, e.g. GDF-15 (ng/l), NT-pro BNP (ng/l), Troponin (ng/l) and related markers in case group compared to controls

    Time frame: 4 years

  5. Number of neonates with adverse neonatal outcome

    A composite measure for neonatal outcome will be created using information on fetal acidemia, Apgar-score, asphyxia, intra-/postpartum fetal death, neonatal intubation/mechanical ventilation, meconium aspiration syndrome, netonatal hypoxic-ishcemic encephalopathy, therapeutic hypothermia of the neonate, rate of acute cesarean section (due to suspected fetal distress) and compared in case group and controls

    Time frame: 4 years

Secondary outcomes

  1. Number of participants with operative vaginal delivery due to suspected fetal distress

    Rates of operative vaginal deliveries (forceps/vacuum/combined; due to suspected fetal distress) in case and control groups

    Time frame: 4 years

  2. Percentage of participants with pathological placenta histology findings in case and control groups

    As assessed by a senior perinatal pathologist using predefined criteria

    Time frame: 4 years

06

Study locations

1 site
  • Oslo University Hospital
    Oslo, 0407, Norway
07

References and documents

Individual participant data

Plan to share: Undecided — Depending on when the permission for the dataset usage for the project's outcome measures ends (OUH personal data officer/Regional Ethical Comittee) AND Norwegian legislation regarding personal data protection. It is unlikely that a major part of the data set will be shared openly due to these restrictions on sensitive personal data matters.

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT05872009
Lead sponsor
Oslo University Hospital
Collaborators
Norwegian SIDS and Stillbirth Society
Responsible party
Meryam Sugulle (Principal Investigator, Oslo University Hospital) — Principal investigator
First posted
May 23, 2023
Start date
Jun 1, 2023 (estimated)
Primary completion
Jun 2026 (estimated)
Completion
Jun 2026 (estimated)
Last update
May 23, 2023

Study contacts

Meryam Sugulle, PhD
Contact
UXSUME@ous-hf.no
+47 22119800
Bendik Fiskå, M.D.
Contact
benfis@ous-hf.no
+47 22119800
Meryam Sugulle, PhD
principal investigator · Oslo University Hospital, Division of Gynaecology and Obstetrics, Ullevål

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in May 2023. You cannot join it, but the record below documents what was studied.

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