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Enrolling By InvitationNCT07163156

Prolactin, Inflammation, and Parkinson's Severity

The Relationship of Prolactin and Inflammatory Markers With Parkinson's Disease Severity: Clinical and Biochemical Evaluation

Status
Enrolling By Invitation
Phase
Study type
Observational
Enrollment
300 (estimated)
Sponsor
Çanakkale Onsekiz Mart University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers

Summary

This cross-sectional observational study aims to evaluate the relationship between serum prolactin levels, peripheral inflammatory markers (NLR, PLR, SII, CRP), and disease severity in patients with Parkinson's disease (PD). A total of at least 300 patients diagnosed with idiopathic PD will be included. Disease severity will be assessed using the Unified Parkinson's Disease Rating Scale (UPDRS) and the Modified Hoehn-Yahr staging system. Serum and salivary prolactin levels will be measured using ELISA, while inflammatory markers will be calculated from routine blood tests. The study seeks to clarify whether prolactin and systemic inflammation indicators may serve as non-invasive biomarkers for disease progression and prognosis in PD, with particular emphasis on postmenopausal women.

Conditions

Timeline

Start date
2025-08-14
Primary completion
2025-12-01
Completion
2026-06-01
First posted
2025-09-09
Last updated
2025-09-09

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT07163156. Inclusion in this directory is not an endorsement.

Prolactin, Inflammation, and Parkinson's Severity (NCT07163156) · Clinical Trials Directory