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Effect of plasma adsorption therapy in amyotrophic lateral sclerosis

A Short-term Outcome of Plasma Adsorption Therapy of Amyotrophic Lateral Sclerosis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN22850763
Enrollment
28
Registered
2017-09-20
Start date
2015-09-01
Completion date
Unknown
Last updated
2017-10-09

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

Conditions

Amyotrophic Lateral Sclerosis Musculoskeletal Diseases Amyotrophic Lateral Sclerosis

Interventions

All patients received plasma adsorption once a week for three successive times. For each treatment, blood flow was 80-120mL/min and the slurry velocity was 1.5 L/h. One and a half times of the Plasma

Sponsors

The Third Affiliated Hospital of Southern Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Upper and lower motor neuron signs in three regions 2. Any age or gender

Exclusion criteria

Exclusion criteria: 1. Allergic to membranes or pipelines of plasma separator and adsorber 2. Severe active bleeding or DIC; Systemic circulatory failure which do not respond well to treatment 3. Unstable myocardial or cerebral infarction, intracranial hemorrhage or severe brain edema with cerebral hernia 4. Incoordination due to psychonosema

Design outcomes

Primary

MeasureTime frame
1. Clinical manifestations of ALS patients is measured using the physical examination at one week after treatment 2. Function evaluation is measured using ALSFR-S scores at one week after treatment 3. Serum creatine kinase (CK) and serum lactate dehydrogenase (LDH) at one week after treatment

Secondary

MeasureTime frame
No secondary outcome measures

Countries

China

Contacts

Public ContactShulu;Bin Zhou;Li

;

1693494745@qq.com;250001820@qq.com+86 13926227269;+86 13660196991

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026