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Delipid Extracorporeal Lipoprotein Filter From Plasma (DELP) for Acute Hemorrhagic Stroke

Delipid Extracorporeal Lipoprotein Filter From Plasma (DELP) for Acute Hemorrhagic Stroke: a Prospective, Random, Open-label, Blind-endpoint, Multi-centre Study

Status
Suspended
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05128513
Enrollment
356
Registered
2021-11-22
Start date
2022-01-14
Completion date
2027-04-08
Last updated
2026-04-23

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

Conditions

Hemorrhagic Stroke

Brief summary

Delipid Extracorporeal Lipoprotein filter from Plasma (DELP) has been found to improve neurological function and life ability of AIS patients and approved for the treatment of AIS by China Food and Drug Administration (CFDA). A recent study imply that the neuroprotective effect of DELP involved multiple neuroprotective mechanism such as anti-inflammation, free radical scavenging, and decreasing MMP-9. Based on the multiple mechanisms, the investigator argues that DELP may exert neuroprotective effect on acute cerebral hemorrhage (ACH). In this context, the prospective, random, open-label, blind-endpoint, multi-centre study is designed.

Interventions

DEVICEDELP

The blood was pumped into the PCS2 plasma separator through one side of the forearm vein. The plasma was separated by pump and then sent to the DELP system (Shanghai Jiangxia Blood Technology Co.). After purification, the plasma was returned to the patient via another forearm vein. The total treatment plasma volume was 800-1,000 mL; the anticoagulant 4% sodium citrate dehydrate solution with a ratio of 1:16 to plasma, was dropped before pumping. To prevent hypocalcemia, 500 mg CaCl2 diluted with 250 mL physiological saline was infused at a rate of 150 mL/h, in the first cycle of the returning blood transfusion.

Sponsors

General Hospital of Shenyang Military Region
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Age: 18-80; * Spontaneous cerebral hemorrhage; * Deep supratentorial intracerebral hemorrhage (basal ganglia) with hematoma volume 5-40ml, or supratentorial lobar hemorrhages with hematoma volume 5-30ml; * NIHSS: 6-20; * Time from onset to DELP: 6-48 hours; * Premorbid mRS 0 or 1; * Signed informed consent;

Exclusion criteria

* Secondary cerebral hemorrhage (secondary to trauma, tumor, vascular malformation, hemorrhage transformation of ischemic stroke, etc.); * Comatose patients on admission (GCS score 3-8 on the Glasgow Coma Scale); * Patients with intracerebral hemorrhage ruptured into the ventricle, which should be treated by surgery; * Planed surgery; * Severe hepatic or renal dysfunction, increase in ALT or AST (more than 2 times of upper limit of normal value), increase in serum creatinine (more than 1.5 times of upper limit of normal value) or requiring dialysis; * Severe hypertension (systolic blood pressure over 200mmHg or diastolic blood pressure over 110 mmHg), or hypotension (systolic blood pressure below 90mmHg or diastolic blood pressure below 60 mmHg); * Previous allergy to heparin or calcium; * Life expectancy is less than 6 months due to comorbidity * Infected at the venipuncture site * hypoproteinemia; * Unsuitable for this clinical studies assessed by researcher.

Design outcomes

Primary

MeasureTime frameDescription
Proportion of patients with modified Rankin Score 0 to 2Day 90the minimum and maximum values of modified Rankin Score are 0 and 6, respectively; higher score mean a worse outcome

Secondary

MeasureTime frameDescription
Proportion of patients with modified Rankin Score 0 to 1Day 90the minimum and maximum values of modified Rankin Score are 0 and 6, respectively; higher score mean a worse outcome
distribution of modified Rankin ScoreDay 90the minimum and maximum values of modified Rankin Score are 0 and 6, respectively; higher score mean a worse outcome
Changes in National Institute of Health stroke scale (NIHSS)24 hours and 2 weeksthe minimum and maximum values of NIHSS are 0 and 42, respectively; higher NIHSS mean a worse outcome
the occurence of stroke or other vascular eventsDay 90
the changes in cerebral hematoma volume24 hoursthe hematoma volume was formulated by brain CT
the severe adverse events24 hours
the occurence of death due to any cause2 weeks

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 24, 2026