Clinical Trials Directory

Trials / Completed

CompletedNCT06529588

Estimation of (suPAR) in Chronic Periodontitis With Post-radiotherapy on HNCs Patients

Soluble Urokinase Plasminogen Activator Receptor (suPAR) is a Potential Biomarker of Stage III-IV, Grade C Periodontitis Through the Impact of Post-radiotherapy on Head and Neck Cancer Patients

Status
Completed
Phase
Study type
Observational
Enrollment
150 (actual)
Sponsor
Al-Maarif University College · Academic / Other
Sex
All
Age
28 Years – 65 Years
Healthy volunteers
Accepted

Summary

This study aims to improve a soluble urokinase plasminogen activator receptor suPAR is a reliable biomarker of chronic periodontitis and may be replaced in patients with head and neck cancer post-radiotherapy (HNC post-RT).

Detailed description

The urokinase-type plasminogen activator receptor (uPAR) plays an essential function in leukocytes and endothelial homeostasis and, therefore, in the development of chronic periodontitis. The study enrolled 150 participants, 50 chronic periodontitis with head and neck cancer post radiotherapy (CP+HNC post-RT) patients, 50 chronic periodontitis (CP) without HNC patients, and 50 healthy controls. Clinical Attachment Loss (CAL), Probing Pocket Depth (PPD), Plaque Index (PI), and Gingival Bleeding Index (GBI) were recorded. An enzyme-linked immunosorbent assay (ELISA) was constructed to quantify serum (suPAR) levels.

Conditions

Interventions

TypeNameDescription
RADIATIONRadiationHNCs patients who received radiotherapy was exposure (5700-7000 Gys) for fractions number (32-35) after 6 months

Timeline

Start date
2022-09-01
Primary completion
2023-01-09
Completion
2023-10-23
First posted
2024-07-31
Last updated
2024-07-31

Locations

1 site across 1 country: Iraq

Source: ClinicalTrials.gov record NCT06529588. Inclusion in this directory is not an endorsement.