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Egg White-Based Snack Improves Serum Albumin and Nutritional Intake in CAPD Patients: A Single-Arm Intervention Study

Effect of a High-Protein, Low-Sodium Egg White-Based Nutritional Snack on Serum Albumin and Dietary Intake in Continuous Ambulatory Peritoneal Dialysis (CAPD) Patients: A Single-Arm Intervention Study

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20250727001
Enrollment
42
Registered
2025-07-27
Start date
2023-10-09
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

End-stage renal disease Peritoneal dialysis Protein-energy wasting Hypoalbuminemia Malnutrition Nutritional supplementation Chronic kidney disease Dietary protein intake Peritoneal Dialysis Renal Insufficiency, Chronic Protein-Energy Malnutrition Dietary Proteins Egg Proteins Nutritional Status Serum Albumin Dietary Supplements

Interventions

Participants received a high-protein, low-sodium egg white-based nutritional product (Egg Bite) as a dietary supplement. Each participant consumed three sachets per day (total 105 g), providing 390 kc
Intervention: Egg Bite

Sponsors

The primary sponsor of this study is Technology and Innovation-Based Enterprise Development Fund (TED Fund) Project Proof of Concept (POC)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Patients aged 18 years or older 2. Diagnosed with end-stage renal disease (ESRD) 3. Undergoing continuous ambulatory peritoneal dialysis (CAPD) for at least 3 months 4. Able to consume oral nutritional supplements 5. Serum albumin level less than or equal to 3.8 g/dL at screening 6. Willing to comply with the 21-day intervention protocol

Exclusion criteria

Exclusion criteria: 1. History of allergy to eggs or egg products 2. Diagnosed with liver cirrhosis or severe hepatic impairment 3. Active infection or hospitalization within the past 1 month 4. Participation in another clinical trial within the past 30 days 5. Pregnant or breastfeeding at the time of enrollment 6. Cognitive impairment or psychiatric disorders interfering with study compliance 7. Uncontrolled diabetes mellitus (fasting plasma glucose >200 mg/dL)

Design outcomes

Primary

MeasureTime frame
Serum albumin concentration, daily protein intake, blood urea nitrogen, prealbumin, hs-CRP Baseline, Day 14, and Day 21 Enzymatic colorimetric method using an automated clinical chemistry analyzer

Secondary

MeasureTime frame
body weight, fasting plasma glucose Baseline, Day 14, and Day 21 Enzymatic colorimetric method using an automated clinical chemistry analyzer

Countries

Thailand

Contacts

Public ContactWittawas Sajjapong

University of Phayao, School of Medical Sciences, Division of Nutrition and Dietetics

wittawas.sa@up.ac.th054466666

Outcome results

None listed

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