Evaluation of sFlt-1/PlGF Ratio ,OPG and sEng as Predictive Biomarkers in the Diagnosis and Treatment Evaluation of Preeclampsia

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18-45
SponsorAmmar Jassim Abed

About this trial

his study investigates the effectiveness of three specific biological markers (biomarkers) in the blood-the sFlt-1/PlGF ratio, soluble endoglin (sEng), and osteoprotegerin (OPG)-to better diagnose and monitor preeclampsia. Preeclampsia is a serious pregnancy complication characterized by high blood pressure and potential organ damage that affects 2-8% of pregnancies worldwide

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Pregnant women between 20 and 36 weeks of gestation

Age between 18 and 45 years

Attending the antenatal clinic at the study site

Disqualifiers

Chronic hypertension

Renal disease

Diabetes mellitus

Multiple gestations

Trial population

he study population will include pregnant women aged 18-45 years, between 20 and 36 weeks of gestation, attending the antenatal clinic at the study site. Participants will be divided into three groups: Pregnant women diagnosed with preeclampsia who have not yet received antihypertensive treatment. Pregnant women diagnosed with preeclampsia who are receiving antihypertensive treatment. Healthy pregnant women serving as control subjects. Exclusion criteria include pre-existing chronic hypertension, renal disease, diabetes mellitus, multiple gestations, or autoimmune disorders. All participants will provide informed consent before enrollment. Blood samples will be collected for biomarker analysis (sFlt-1, PlGF, soluble endoglin, and osteoprotegerin). This population has been selected to allow comparison of biomarker levels in different clinical scenarios and to evaluate their

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

120 Participants
are grouped into 3 trial groups
Group A: Preeclampsia - No Antihypertensive Treatment
Group B: Preeclampsia - With Antihypertensive Treatment
Group C: Healthy Pregnant Controls

Trial outcomes

Primary outcomes

1

Serum sFlt-1 concentration

Measurement of serum sFlt-1 levels in maternal serum using ELISA

Time frame
At enrollment (20-36 weeks of gestation)
2

Serum PlGF concentration

Measurement of serum placental growth factor (PlGF) levels in maternal serum using ELISA.

Time frame
At enrollment (20-36 weeks of gestation)
3

sFlt-1/PlGF ratio

Calculated ratio of serum sFlt-1 to serum PlGF concentrations

Time frame
At enrollment (20-36 weeks of gestation)
4

Serum Osteoprotegerin (OPG) concentration

Measurement of serum osteoprotegerin (OPG) levels in maternal serum using ELISA.

Time frame
At enrollment (20-36 weeks of gestation)

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Ammar Jassim Abed

Lead sponsor

University of Thi-Qar

Sponsor institution