Viewing Study NCT04830332



Ignite Creation Date: 2024-05-06 @ 4:00 PM
Last Modification Date: 2024-10-26 @ 2:01 PM
Study NCT ID: NCT04830332
Status: COMPLETED
Last Update Posted: 2021-04-05
First Post: 2021-03-31

Brief Title: Correlation of Peritoneal Fluid CA-125 Levels With Postoperative Tumor Histology
Sponsor: Erdemli State Hospital
Organization: Erdemli State Hospital

Study Overview

Official Title: Correlation of Preoperative Serum and Intraoperative Peritoneal Washing Fluid CA-125 Levels With Postoperative Tumor Histology in Patients With Endometrial Carcinoma a Prospective-controlled Study
Status: COMPLETED
Status Verified Date: 2021-03
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: In this prospective study we aimed to investigate whether serum and abdominal washing fluid CA-125 levels correlated with postoperative histopathological parameters in patients with endometrial carcinoma
Detailed Description: Endometrial cancer was diagnosed with histopathological examination of the samples obtained by dilatation and curettage Preoperative serum CA-125 levels were determined in all patients Serum and abdominal washing fluid CA-125 levels were measured with a double antibody sandwich immunoenzymatic method using Beckman Coulter DXI Ireland analyzer In addition to routine preoperative investigations MRI was done in patients who were thought to have an extension outside the uterus

During surgery abdominal exploration was performed first and then an abdominal fluid sample was obtained for cytological examination and measurement of CA-125 level One hundred milliliters of normal saline was used as the abdominal washing liquid to obtain the sample for CA-125 measurement Subsequently total abdominal hysterectomy and bilateral salpingo-oophorectomy TAH BSO were performed

Study Oversight

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