Viewing Study NCT06487767



Ignite Creation Date: 2024-07-17 @ 12:03 PM
Last Modification Date: 2024-10-26 @ 3:34 PM
Study NCT ID: NCT06487767
Status: NOT_YET_RECRUITING
Last Update Posted: 2024-07-05
First Post: 2024-06-27

Brief Title: The Validity of the Use of Imaging in Cervical Cancer Staging
Sponsor: University of Pretoria
Organization: University of Pretoria

Study Overview

Official Title: The Validity of the Use of Imaging in Cervical Cancer Staging
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-06
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: The study wil aim to investigate the accuracy of imaging in the staging of women diagnosed with cervical cancer
Detailed Description: Patients with cervical cancer undergoing surgery will also undergo PET-CT scan CT scan trans-abdominal ultrasound of the pelvis and abdomen to assess pelvic and para-aortic lymph node status MRI and trans-vaginal ultrasound TVUS to assess tumour size and parametrial infiltration As per the current unit protocol patients will be assessed clinically for operability The performance of the different imaging modalities will be measured against the histological status of the parametric and lymph nodes and tumour size as measured by the pathologists

CT PET-CT MRI and abdominal ultrasound will be reported as per the usual departmental process Staff in the radiology department will be blinded for the different imaging modalities performed TVUS will be performed in the unit by different gynaecological oncologists and fellows and at the time of the investigation will be blinded with regards to clinical findings and the reports of other imaging studies performed

The sensitivity specificity positive and negative predictive values will be calculated for the different imaging modalities

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