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Clinical study of continuous blood purification in treatment of neonatal capillary leakage syndrome

Clinical study of continuous blood purification in treatment of neonatal capillary leakage syndrome

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300068255
Enrollment
Unknown
Registered
2023-02-13
Start date
2023-02-13
Completion date
Unknown
Last updated
2023-05-22

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

Conditions

Capillary leakage syndrome

Interventions

control group:The delayed initiation of CBP strategy group was given the basic treatment of CLS, but when the existing treatment failed, that is, CBP therapy was initiated when the following condition
Experimental group:n the early initiation of CBP strategy group, once CLS was diagnosed, CBP therapy was initiated under the original basic treatment regimen

Sponsors

Jiangxi Maternal and Child Health Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged = 1000 g, <= 2000 g; 3. It meets the diagnostic criteria of neonatal capillary leakage syndrome. Diagnostic criteria for CLS: The diagnosis is mainly based on clinical manifestations, that is, the existence of definite inducing factors (different from systemic CLS without definite inducing factors); Physical examination: body mass increased by more than 3% within 24 h, systemic skin mucosal edema, bulbar conjunctival edema, blood pressure and central venous pressure decreased, or accompanied by pleuroperitoneal effusion and pericardial effusion; Laboratory examination: hypoproteinemia (< 25 g/L), edema aggravated after supplementing small molecule crystal substance, increased blood concentration or hematocrit (HCT), urine trace protein positive, decreased blood-oxygen binding ability, X-ray showed exudative changes in lung interstitium.

Exclusion criteria

Exclusion criteria: 1. Cardiogenic, nephrogenic, hepatogenic edema, genetic metabolic diseases, and congenital malformations (such as complex congenital heart disease or congenital heart disease with severe hemodynamic changes, chromosome abnormalities, fetal edema, etc.); 2. There are other serious life threatening complications: pulmonary hemorrhage, grade 3-4 intracranial hemorrhage, severe pulmonary hypertension (reaching the guideline for the application of ECMO).

Design outcomes

Primary

MeasureTime frame
Mental state;Skin temperature;Skin color;Capillary refill time;Blood pressure;Changes in pulse rate;Shock index;Changes in urine volume;Central venous pressure;Cardiac index;Blood gas analysis;Blood lactic acid;Coagulation function;Serum creatinine;Urea nitrogen;Duration of hypotension;Duration of edema;Duration of oliguria;The duration of vasoactive drug use;

Secondary

MeasureTime frame
The duration of the ventilator;Time to start enteral feeding;Survival rate;complication;

Countries

China

Contacts

Public ContactLi Xu

Jiangxi Maternal and Child Health Hospital

552091588@qq.com+86 158 7911 2297

Outcome results

None listed

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