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Pepsinogen-1 Serum Levels in Hyperemesis Gravidarum

A

Ankara Etlik City Hospital

Status

Completed

Conditions

Pregnant With Complication
Hyperemesis Gravidarum

Treatments

Other: pepsinogen-1

Study type

Observational

Funder types

Other

Identifiers

NCT06581796
AECH-FIRATLIGIL-002

Details and patient eligibility

About

In this study, the investigators planned to investigate maternal serum pepsinogen-1 (MSPG-1) levels in pregnant women with severe hyperemesis gravidarum (HG) and pregnant women without severe HG.

HG is the most common cause of hospitalization in the first trimester of pregnancy and represents an economic burden on the healthcare system. Therefore, our aim in this study was to investigate whether there is a statistical difference in MSPG-1 levels between pregnant women with severe HG and pregnant women without severe HG and to determine a cut-off value for MSPG-1 levels for the indication of hospitalization of pregnant women with HG.

The study poses no risk to the pregnant woman or the fetus.

Full description

The study will enroll pregnant women in the first trimester with maternal age between 21 and 35 years who were diagnosed with hyperemesis gravidarum and had no fetal congenital or chromosomal abnormalities and who were admitted to the perinatology outpatient clinic of Etlik City Hospital. The investigators will include 40 cases with no signs and diagnosis of systemic maternal disease and no chronic drug use as a case group and 40 healthy pregnant women matched for age, gestational week and body mass index as a control group.

Enrollment

40 patients

Sex

Female

Ages

21 to 35 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • A singleton pregnancy
  • Between 21 and 35 years old
  • Diagnosis of hyperemesis gravidarum

Exclusion criteria

  • Multiple pregnancy
  • Fetal congenital and chromosomal abnormalities
  • Chronic drug use, alcohol and smoking
  • Pregnant women with diabetes or obesity, peptic ulcer or gastritis, liver and/or gallbladder disease (cholangitis or gallstones), thyroid dysfunction, urinary tract infection, celiac disease, cardiovascular or renal disease

Trial design

40 participants in 2 patient groups

Study group
Description:
pregnant women with hyperemesis gravidarum
Treatment:
Other: pepsinogen-1
Control group
Description:
pregnant women without hyperemesis gravidarum
Treatment:
Other: pepsinogen-1

Trial contacts and locations

1

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Central trial contact

Sadun Sucu, MD; Fahri B Firatligil, MD

Data sourced from clinicaltrials.gov

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