About this trial
Background Frailty is an age-related syndrome characterized by reduced physiological reserve, decreased stress tolerance and multisystem functional decline in the elderly, which markedly increases the risks of falls, hospitalization, functional impairment and all-cause mortality. Chronic low-grade inflammation, immune senescence, oxidative stress and abnormal protein modification are key mechanisms underlying the development and progression of frailty. Current mainstream interventions including nutritional support and physical exercise yield limited efficacy for moderate to severe frailty, and targeted therapies against biological aging mechanisms are still lacking.Objective To evaluate the efficacy and safety of plasma exchange combined with human albumin (ALB), with or without intravenous immunoglobulin (IVIg), in the treatment of frailty, and to preliminarily explore the potential mechanisms of the combined therapy.Methods This is a prospective, randomized, exploratory clinical trial. A total of 34 participants with a FRAIL scale score ≥ 1 will be enrolled and randomly assigned at a 1:1 ratio into two groups, with 17 cases in each group: the plasma exchange plus ALB group and the plasma exchange plus ALB plus IVIg group. The study consists of a screening phase, a 5-month treatment phase with six intervention sessions, and follow-up visits at 1, 3 and 6 months after the final treatment. Frailty status, physical function, laboratory parameters, inflammatory levels and albumin modification will be dynamically assessed throughout the trial, and adverse events will be recorded.Results The trial has not yet been initiated. It is expected that the within-group and between-group comparisons will clarify the therapeutic effects and long-term stability of the two regimens, as well as their safety profiles. Changes in biomarkers will help illustrate the potential molecular mechanisms of plasma purification combined with functional protein supplementation for frailty.Conclusion Plasma exchange combined with ALB (with or without IVIg) can exert multi-target intervention on frailty by eliminating aging-related toxic factors and restoring plasma and immune homeostasis. The findings of this study will provide preliminary clinical evidence and theoretical basis for novel biological therapeutic strategies for frailty.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Age ≥ 18 years.
Clear consciousness and ability to communicate.
Sufficient cognitive function and educational level to complete all study-related assessments.
A score of ≥ 1 on the FRAIL scale.
Disqualifiers
Known allergy or hypersensitivity to albumin (ALB) or intravenous immunoglobulin (IVIg).
Currently receiving albumin (ALB) and/or intravenous immunoglobulin (IVIg) infusion for other reasons.
Severe cardiac, hepatic, or renal insufficiency.
Active infection or acute exacerbation of chronic infection.
Trial design
Parallel
Treatments tested in this trial
Plasma Exchange
Procedure/SurgeryPlasma exchange procedure, target exchange volume 50±5 mL/kg per session, flow rate 40-60 mL/min, administered once monthly for 6 cycles.
5% human albumin
Biological/VaccineEqual-volume 5% human albumin solution used as replacement fluid during plasma exchange.
Intravenous immunoglobulin (IVIG)
Biological/VaccineIVIg administered at a fixed dose of 2.5 g per subject, infused immediately after each plasma exchange session.
Treatment groups
Trial outcomes
Primary outcomes
Efficacy rate of frailty intervention at 1 month after the last treatment
Calculation formula: \[(Baseline score - Follow-up score at 1 month after the last treatment) / Baseline score\] × 100%. This rate represents the degree of improvement in patients' frailty status following intervention.
Secondary outcomes
Efficacy rate of frailty intervention assessed by FRAIL Scale
The efficacy rate of frailty intervention calculated based on the FRAIL Scale (Fatigue, Resistance, Ambulation, Illnesses, Loss of weight). The scale ranges from 0 (no frailty) to 5 (severe frailty); higher scores indicate worse frailty status. Efficacy rate = (Baseline score - Score at follow-up) / Baseline score × 100%.
Strand specificity of frailty-related cfDNA and therapeutic response to plasma exchange
Assess strand specificity of frailty-related circulating cell-free DNA and evaluate its predictive value for plasma exchange treatment response.
Clonal hematopoiesis gene mutation dynamics and correlation with frailty
Observe clonal hematopoiesis-associated gene mutation and clonal evolution at baseline, 1 month and 6 months post last treatment; explore the correlation between clonal hematopoiesis features and frailty status.
BCR clonotype characteristics
Analysis of BCR clonotype derived from identical BCR high-throughput sequencing assay. Assessments are performed at baseline, 1 month and 6 months after the last treatment.
Sponsors and contacts
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