The Role of Pentraxin 3 and Cathepsin B Levels in Preeclamptic Pregnancy

Sponsor
Sanliurfa Mehmet Akif Inan Education and Research Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT05924061
Collaborator
(none)
156
1
12
13

Study Details

Study Description

Brief Summary

In this study, the investigator aim was to compare Cathepsin B and Pentraxin 3 levels measured from maternal serum of pregnant women diagnosed with preeclampsia in the second trimester, the effects of these levels on maternal/ fetal outcomes and the composite results of Cathepsin B and Pentraxin 3 levels alone or together and contribute to the literature in this area.

Condition or Disease Intervention/Treatment Phase
  • Other: Cathepsin B and pentraxin 3 levels in preeclampsia with pregnant women

Detailed Description

This prospective case-control study was conducted between 1 January 2022 and 31 December 2022 at Bursa Yuksek Ihtisas Training and Research Hospital. The study was conducted with pregnant women between ages of 18-45 who were diagnosed with preeclampsia in the second trimester. This study was conducted with total 156 pregnant women. participants were grouped according to the presence of preeclampsia; Group1: Patients diagnosed with preeclampsia between 20-28 weeks (study group) (n:78) , Group 2: Healthy pregnant women between 20-28 weeks without a diagnosis of preeclampsia ( control group) (n:78) . As soon as preeclampsia is diagnosed and before any treatment was started, maternal serum samples were collected in the Cathepsin B and Pentraxin 3 kit in amounts suitable for the study. The samples obtained were kept in biochemistry laboratory at -80 degrees until the study was conducted. After all samples were collected, Cathepsin B and Pentraxin 3 values were measured by ELISA method.

Study Design

Study Type:
Observational [Patient Registry]
Actual Enrollment :
156 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
The Role of Pentraxin 3 and Cathepsin B Levels in the Second Trimester in Predicting of Maternal and Fetal Results in Preeclamptic Pregnancy
Actual Study Start Date :
Jan 1, 2022
Actual Primary Completion Date :
Dec 31, 2022
Actual Study Completion Date :
Dec 31, 2022

Arms and Interventions

Arm Intervention/Treatment
Pregnant women with preeclampsia between 20-28 weeks (study group)

Maternal serum cathepsin B and pentraxin 3 levels in 20-28 weeks pregnant women with preeclampsia

Other: Cathepsin B and pentraxin 3 levels in preeclampsia with pregnant women
The effect of cathepsin b and pentraxin 3 levels on maternal/fetal outcomes in pregnant women diagnosed with preeclampsia

Healthy pregnant women between 20-28 weeks ( control group)

Maternal serum cathepsin B and pentraxin 3 levels in 20-28 weeks healthy pregnant women ( control group)

Other: Cathepsin B and pentraxin 3 levels in preeclampsia with pregnant women
The effect of cathepsin b and pentraxin 3 levels on maternal/fetal outcomes in pregnant women diagnosed with preeclampsia

Outcome Measures

Primary Outcome Measures

  1. Comparison of the effects and composite results of cathepsin b and pentraxin 3 levels in pregnant women diagnosed with preeclampsia [12 months]

    serum cathepsin b (nmoL pNA/mL) and serum pentraxin 3 (ng/ml) levels composite results on pregnant women diagnosed with preeclampsia

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 45 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Singleton pregnancy

  • Pregnant women diagnosed with preeclampsia between 20-28 weeks of gestation

  • Healthy pregnant women between 20-28 weeks of gestation who want to be involved in the study.

Exclusion Criteria:
  • Multiple pregnancies

  • Pregnant women who gave birth below 24 weeks of gestation

  • Pregnant women diagnosed with other hypertensive diseases of pregnancy other than preeclampsia ( gestational hypertension, chronic hypertension, superimposed hypertension)

  • Pregnant women with chromosomal or congenital anomalies in the fetus

  • Women with a known infective or autoimmune disease before pregnancy

Contacts and Locations

Locations

Site City State Country Postal Code
1 Nefise Nazlı YENIGUL Bursa Turkey 16110

Sponsors and Collaborators

  • Sanliurfa Mehmet Akif Inan Education and Research Hospital

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Nefise Nazlı YENIGUL, Ph.D. Assistant Professor Department of Obstetrics and Gynecology, Sanliurfa Mehmet Akif Inan Education and Research Hospital
ClinicalTrials.gov Identifier:
NCT05924061
Other Study ID Numbers:
  • 2011-KAEK-25 2021/09-09
First Posted:
Jun 29, 2023
Last Update Posted:
Jun 29, 2023
Last Verified:
Jun 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Nefise Nazlı YENIGUL, Ph.D. Assistant Professor Department of Obstetrics and Gynecology, Sanliurfa Mehmet Akif Inan Education and Research Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 29, 2023