Viewing Study NCT06623942



Ignite Creation Date: 2024-10-26 @ 3:41 PM
Last Modification Date: 2024-10-26 @ 3:41 PM
Study NCT ID: NCT06623942
Status: COMPLETED
Last Update Posted: None
First Post: 2024-09-24

Brief Title: Prostasin Levels in Preeclamptic Women
Sponsor: None
Organization: None

Study Overview

Official Title: Prostasin Levels in Preeclampsia A Comparative Study With Healthy Pregnancies
Status: COMPLETED
Status Verified Date: 2024-09
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This study will aim to compare maternal serum prostasin levels between women diagnosed with preeclampsia and healthy normotensive pregnant controls Participants will be divided into two main groups those with preeclampsia and those with uncomplicated pregnancies The preeclampsia group will further be subdivided based on the severity of the condition Maternal serum samples will be collected from all participants and prostasin levels will be measured using ELISA Statistical analyses will be performed to evaluate whether prostasin levels are significantly elevated in the preeclampsia group particularly in those with severe features and to assess its potential as a biomarker for the condition
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None