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DASH Diet, Triglycerides and AIP in Parkinson's Disease

A

Abant Izzet Baysal University

Status

Completed

Conditions

Parkinson's Disease

Treatments

Other: No intervention (observational study)

Study type

Observational

Funder types

Other

Identifiers

NCT07402993
AIBU-BD-NKÖ-04

Details and patient eligibility

About

Participants who agreed to participate in the study were informed about the purpose of the research and obtained their consent to participate in the study using an informed consent form. The study was conducted on 70 patients with Parkinson's disease. Participants who volunteered to participate in the study were given a questionnaire form containing sociodemographic characteristics. In addition, participants' anthropometric measurements (body weight, height, waist and hip circumference, Body Mass Index (BMI)), biochemical parameters (fasting blood glucose, HbA1c, triglycerides, LDL cholesterol, triglycerides, total cholesterol, C-reactive protein (CRP), albumin, and hematology markers (hemoglobin (Hb), hematocrit (Htc), leukocytes and platelets, lymphocytes) and serum vitamin D, folic acid, vitamin B12) and nutritional status (food consumption frequency, DASH diet compliance) were obtained. New cardiovascular risk markers such as neutrophil/lymphocyte ratio (NLR), monocyte HDL ratio (MHR), and plasma atherogenic index (PAI) were calculated.

Enrollment

70 patients

Sex

All

Ages

19+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Individuals over 19 years of age
  • Individuals who are literate
  • Individuals diagnosed with Parkinson's Disease

Exclusion criteria

  • Individuals who have had an acute infection or inflammatory disease within the past month
  • Individuals with chronic infectious or inflammatory diseases
  • Individuals with cancer

Trial design

70 participants in 1 patient group

Individuals with Parkinson's disease
Description:
This cohort includes adult participants diagnosed with Parkinson's disease. No control group is included.
Treatment:
Other: No intervention (observational study)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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