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Effects of Omega 3 Fatty Acids on Reduction of Arterial Stiffness in Peritoneal Dialysis Patients

Effects of Omega 3 Fatty Acids on Reduction of Arterial Stiffness in Peritoneal Dialysis Patients: A Randomized Control Trial

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20251230002
Enrollment
60
Registered
2025-12-30
Start date
2021-08-28
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Arterial stiffness in peritoneal dialysis patients peritoneal dialysis chronic kidney disease omega-3 fatty acids arterial stiffness cardio-ankle vascular index (CAVI) pulse wave velocity

Interventions

The intervention arm received omega 3 fatty acids, Omacor, at a dose of 2 grams per day for 12 weeks. Each 1 gram capsule contained EPA ethyl esters 450 mg and DHA ethyl ester 380 mg.,The control arm
Experimental Drug,Placebo Comparator Drug
Omega 3 fatty acids ,Control

Sponsors

Navamindradhiraj University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. age more than 18 years old 2. on peritoneal dialysis for at least 3 months

Exclusion criteria

Exclusion criteria: 1. heart failure 2. prior stroke or peripheral arterial disease 3. major surgery or cardiothoracic or vascular surgery within 3 months 4. pregnancy or breastfeeding 5. high bleeding risk (platelet count less than 100,000 per microliter, INR more than 1.5, use of more than 2 antiplatelet or anticoagulant agents, severe or uncontrolled bleeding) 6. allergy to omega-3 fatty acids 7. active metastatic malignancy

Design outcomes

Primary

MeasureTime frame
Change in CAVI from baseline to week 12 12 weeks CAVI using the VaSera VS-1000 system

Secondary

MeasureTime frame
Changes in ba-PWV 12 weeks ba-PWV using an automated waveform analyzer (BP-203RPE II with ST-100E; Colin, model VP-1000) ,Changes in ba-PWV, IL-6, hs-CRP, hemodynamics, lipid profile, and HOMA-IR 12 weeks Blood test,Adverse events 12 weeks Recording reported events

Countries

Thailand

Contacts

Public ContactTeerayut Chitchak

Faculty of Medicine, Navamindradhiraj University

teerayut@nmu.ac.th022443000

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026