Establishment of an Early Warning Screening System for Hemophagocytic Lymphohistiocytosis a Multi-center, Prospective Study

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorThe Affiliated Hospital of Xuzhou Medical University

About this trial

Our three-step screening system uses commonly used clinical and laboratory parameters to effectively identify patients who may be at high risk of HLH, conduct etiology screening early for patients who meet the diagnostic criteria for HLH, and guide standardized treatment. Therefore, this study proposes to establish a highly accurate and convenient hemophagocytic early warning system to improve the early diagnosis of patients with hemophagocytic syndrome and identify suspected HLH patients early. Etiology screening is performed on patients who meet the diagnostic criteria for HLH, high-risk predisposing factors are identified, and precise treatment is guided, thereby improving the success rate of patient treatment and improving the quality of life.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients who meet the first step screening + have ≥ 3 abnormal screening indicators in the second step

Patients who meet the first step screening + have 2 abnormal screening indicators in the second step + patients with high-risk factors for HLH, such as history of lymphoma, EBV infection, autoimmune diseases, etc

Disqualifiers

None

Trial population

A three-step screening process identified 80 people with suspected hemophagocytic syndrome

Trial design

Design model

Case-only

Time perspective

Prospective

Treatments tested in this trial

  • Patients diagnosed with HLH-94 should be treated as soon as possible

    Drug

    For some highly suspicious patients, after diagnosis, according to the patient's etiology, the treatment plan should be determined as soon as possible, such as lymphoma-related patients treated with hormones combined with etoposide, which can greatly improve the prognosis of patients

Treatment groups

80 Participants
are divided into 1 treatment group
Group A: Screening patients with suspected hemophagocytic syndrome1 intervention

Trial outcomes

Primary outcomes

1

The suspected patient was diagnosed with hemophagocytic syndrome after complete NK cell activity, triglyceride tests, etc.

Time frame
Time forecasting:2 years

Secondary outcomes

Other outcomes

Sponsors and contacts

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