A Prospective, Randomized Exploratory Study on the Intervention of Frailty With Human Albumin Combined With Plasma Exchange
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 入组人数
- 34
- 试验地点
- 1
- 主要终点
- Efficacy rate of frailty intervention at 1 month after the last treatment
研究概览
简要总结
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.
详细描述
Frailty is a common age-related clinical syndrome characterized by progressive decline in physiological reserve, reduced stress tolerance, and multisystem functional impairment in older adults. It significantly increases the risk of adverse outcomes including falls, hospitalizations, functional dependence, and all-cause mortality. Chronic low-grade inflammation, immune senescence, oxidative stress, and abnormal protein modification are considered key biological mechanisms driving the onset and progression of frailty. Current mainstream interventions, such as nutritional support and physical exercise, have shown only limited efficacy in moderate to severe frailty, and targeted biological therapies for frailty remain lacking. This study aims to evaluate the efficacy and safety of plasma exchange combined with human albumin (ALB), with or without adjunctive intravenous immunoglobulin (IVIg), in the treatment of frailty, and to preliminarily explore the potential mechanisms underlying the combined therapy.
This is a prospective, randomized, exploratory clinical trial. A total of 34 participants with a FRAIL scale score of ≥ 1 will be enrolled and randomly assigned at a 1:1 ratio into two groups (17 participants in each group): the plasma exchange plus human albumin group (ALB group) and the plasma exchange plus human albumin plus intravenous immunoglobulin group (ALB + IVIg group). The study is divided into three phases: a screening phase, a treatment phase, and a follow-up phase.
The screening phase will be conducted within 7 days prior to the first treatment. Eligible subjects will sign an informed consent form and complete a comprehensive baseline assessment, including frailty status evaluation, physical function testing, routine laboratory and imaging examinations, frailty-related biomarker detection, albumin (ALB) modification profiling, and inflammatory marker testing to confirm eligibility.
The treatment phase will last for 5 months, consisting of a total of 6 treatment sessions administered monthly. Systemic assessments will be performed at each visit, including frailty status evaluation, physical function testing, routine pre-treatment examinations, frailty-related biomarker detection, ALB modification profiling, and inflammatory marker testing, to monitor treatment response and safety. Blood samples for complete blood count and coagulation function will be collected within 1 hour after the first plasma exchange session. All participants will receive plasma exchange with 5% human albumin solution as the replacement fluid, according to the study protocol. Subjects in the ALB + IVIg group will additionally receive intravenous immunoglobulin (IVIg) immediately after each plasma exchange session. Adverse events will be recorded throughout the study.
Follow-up visits will be conducted at 1, 3, and 6 months after the final treatment session. All assessments and laboratory tests will be repeated to evaluate the long-term efficacy, safety, and sustained effects of the interventions.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •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.
- •Voluntary written informed consent.
排除标准
- •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.
- •Current use of direct oral anticoagulants (DOACs).
- •History of bleeding disorders or coagulation dysfunction.
- •Concomitant malignancy or expected survival of less than 6 months.
- •Severe visual, auditory, or motor function impairment.
- •Refusal to sign the informed consent form.
- •Other conditions that, in the opinion of the investigator, make the participant unsuitable for the study.
研究组 & 干预措施
Plasma Exchange + Human Albumin Group
All subjects receive standard background therapy. Subjects receive monthly plasma exchange for 6 cycles with 5% human albumin as replacement fluid, no IVIg administration.
干预措施: Plasma Exchange (Procedure)
Plasma Exchange + Human Albumin Group
All subjects receive standard background therapy. Subjects receive monthly plasma exchange for 6 cycles with 5% human albumin as replacement fluid, no IVIg administration.
干预措施: 5% human albumin (Biological)
Experimental: Plasma Exchange + Human Albumin + IVIg Group
All subjects receive standard background therapy. Subjects receive monthly plasma exchange for 6 cycles with 5% human albumin replacement fluid, plus IVIg 2.5 g after each exchange session.
干预措施: Plasma Exchange (Procedure)
Experimental: Plasma Exchange + Human Albumin + IVIg Group
All subjects receive standard background therapy. Subjects receive monthly plasma exchange for 6 cycles with 5% human albumin replacement fluid, plus IVIg 2.5 g after each exchange session.
干预措施: 5% human albumin (Biological)
Experimental: Plasma Exchange + Human Albumin + IVIg Group
All subjects receive standard background therapy. Subjects receive monthly plasma exchange for 6 cycles with 5% human albumin replacement fluid, plus IVIg 2.5 g after each exchange session.
干预措施: Intravenous immunoglobulin (IVIG) (Biological)
结局指标
主要结局
Efficacy rate of frailty intervention at 1 month after the last treatment
时间窗: 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.
次要结局
- Efficacy rate of frailty intervention assessed by FRAIL Scale(Baseline, 4 week, 8 week, 12 week, 16 week, 20 week, 24 week, 28 week, and 32 week after enrollment)
- Strand specificity of frailty-related cfDNA and therapeutic response to plasma exchange(Baseline, 1 month and 6 months after the last treatment)
- Clonal hematopoiesis gene mutation dynamics and correlation with frailty(Baseline, 4 week,24 week, 28 week, and 32 week after enrollment)
- BCR clonotype characteristics(Baseline, 1 month and 6 months after the last treatment)
- BCR V/J gene usage bias(Baseline, 1 month and 6 months after the last treatment)
- BCR diversity index(Baseline, 1 month and 6 months after the last treatment)
- Frequency of senescence-associated antigen-specific B cell clones(Baseline, 1 month and 6 months after the last treatment)
- TCR clonotype characteristics(Baseline, 1 month and 6 months after the last treatment)
- TCR diversity index(Baseline, 1 month and 6 months after the last treatment)
- TCR V/J gene usage bias(Baseline, 1 month and 6 months after the last treatment)
- Frequency of senescence-associated antigen-specific T cell clones(Baseline, 1 month and 6 months after the last treatment)
- Between-group differences in frailty scale score: ALB group vs ALB+IVIg group(Baseline, 4 week, 8 week, 12 week, 16 week, 20 week, 24 week, 28 week, and 32 week after enrollment)
- Baseline changes of serum ALB modification at 1 month after last treatment(1 month after the last treatment)
- Changes from baseline in senescence-related indicators at 1 month after last treatment(1 month after the last treatment)
- Changes from baseline in Tilburg Frailty Indicator (TFI) scores(Baseline, 4 week, 8 week, 12 week, 16 week, 20 week, 24 week, 28 week, and 32 week after enrollment)
- Changes from baseline in Fried Frailty Phenotype Scale scores(Baseline, 4 week, 8 week, 12 week, 16 week, 20 week, 24 week, 28 week, and 32 week after enrollment)
- Changes from baseline in physical and mental health questionnaire scores(Baseline, 4 week, 8 week, 12 week, 16 week, 20 week, 24 week, 28 week, and 32 week after enrollment)
- Short Physical Performance Battery (SPPB) score(Baseline, 4 week, 8 week, 12 week, 16 week, 20 week, 24 week, 28 week, and 32 week after enrollment)
- Changes in gene mutation frequency and its correlation with immune cell subsets(Baseline, 1 month and 6 months after the last treatment)
- Changes from baseline in CRP(Baseline, 4 week, 24 week, 28 week, and 32 week after enrollment)
- Changes from baseline in ESR levels(Baseline, 4 week, 24 week, 28 week, and 32 week after enrollment)
- Changes from baseline in ferritin levels(Baseline, 4 week, 24 week, 28 week, and 32 week after enrollment)
- Incidence of adverse events during treatment(From initiation of the first treatment through 6-month after completion of all study treatments, assessed up to 12 months)