Yuzuncu Yil University, Faculty of Medicine
Van, Turkey (Türkiye)
NCT Number: NCT06245811
In this study, the relationship between the severity of hyperemesis gravidarum (HEG) disease and subclinical inflammatory factors such as Platelet Crit (PCT), Hemoglobin/red cell distribution width ratio (HRR), Neutrophil/lymphocyte ratio (NLR), was investigated.
Looking for future studies?
Notify Me18 year–45 year
Female
Observational
Van, Turkey (Türkiye)
A total of 215 pregnant women, 102 with hyperemesis gravidarum and 113 healthy pregnant women, were included in the study. HEG patients were divided into three groups according to the modified PUQE classification: mild (n=38), moderate (n=32) and severe (n=32).
In our study, we proposed using a new prognostic marker for HEG patients. We think that our study will be a source for future studies on HEG.
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Smoking, urinary tract infections, previously diagnosed psychological disorders, gastrointestinal disorders, multiple pregnancies, eating disorders, thyroid disorders, inflammatory disease, pregnancy with assisted fertilization technique.
Time frame: 2 months
1: Weight loss of 5% or more since the beginning of pregnancy 2: Vomiting at least three times a day 3: A ketonuria value of +1 or higher on a urinalysis test
Time frame: 2 months
(BMI) (kg/m2) was obtained by dividing body weight (kg) by height (m2) squared
Izzet Celegen
Other
Evaluation of the Relationship Between Hyperemesis Gravidarum (HEG) With Platelet Crit (PCT), Haemoglobin to Red Cell Distribution Width Ratio (HRR) and Neutrophil to Lymphocyte Ratio (NLR).
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07613814
Female Urogenital Diseases and Pregnancy Complications, Hyperemesis Gravidarum
Medan, North Sumatra, Indonesia
View Trial DetailsNCT06581796
Female Urogenital Diseases and Pregnancy Complications, Hyperemesis Gravidarum
Ankara, Yenimahalle, Turkey (Türkiye)
View Trial DetailsNCT04284696
Ascorbic Acid Deficiency, Avitaminosis
Vienna, Austria
View Trial DetailsNCT05098067
Female Urogenital Diseases and Pregnancy Complications, Hyperemesis Gravidarum
Providence, Rhode Island, United States
View Trial Details