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Efficacy of Short Course of Intravenous Dexamethasone and Intravenous Immunoglobulin Therapy in Infection-Related Secondary Hemophagocytic Lymphohistiocytosis (isHLH) (isHLH-IVD/IVIg)
Randomized Controlled Trial to Evaluate and Compare the Efficacy of Short Course of Intravenous Dexamethasone and Intravenous Immunoglobulin Therapy in Infection-Related Secondary Hemophagocytic Lymphohistiocytosis (sHLH)
Rationale/Gaps in Existing Knowledge: Therapy of Infection-associated Secondary Hemophagocytic lymphohistiocytosis (sHLH) in adult lacks evidence from randomized trial guiding first-line immunomodulation and current therapeutic practice primarily extrapolated from decades old pediatric HLH protocols and retrospective studies. In presence of infection very expensive therapy with intravenous Immunoglobulin (IVIG) is preferred over Dexamethasone, however the comparative efficacy of IVIG and Dexamethasone alone remains undefined, especially in resource-constraints settings. (ii) Novelty: This will be among the first randomized controlled trials in adults with infection-associated sHLH, directly comparing efficacy of IVIG with Dexamethasone. The study uniquely integrates clinical outcomes with economic feasibility in a low-middle income setting. (iii) Objectives: Primary objectives will be to compare the efficacy of intravenous (IV) Dexamethasone and IVIG in achieving clinical remission and recovery of HLH-associated cytokines (IL-1, IL-6, TNF-α, IFN-γ, GM-CSF) and Ferritin level. Secondary objectives include assessment of hematologic recovery, adverse events, and short-term mortality. (iv)Method: In this Randomized controlled open-label, non-inferiority clinical trial participants with sHLH, will be allocated (1:1) to receive either short-course of IV Dexamethasone or IVIG along with infection-directed standard care and will be followed-up for 4 weeks to evaluate predefined clinical outcome and laboratory parameters. (v) Expected Outcome: The study aims to establish whether IV Dexamethasone is non-inferior to IVIG for achieving clinical remission, recovery of HLH-associated cytokines level and reduction of short-term mortality. Results are expected to reform evidence-based, cost-effective therapeutic strategies for infection-associated sHLH and improve access to care in resource-constraint healthcare systems.
Studie Overzicht
Toestand
Studietype
Inschrijving (Geschat)
Fase
- Fase 3
Contacten en locaties
Studiecontact
- Naam: Deba Prasad Dhibar, MD
- Telefoonnummer: +911722756670
- E-mail: drdeba_prasad@yahoo.co.in
Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
Accepteert gezonde vrijwilligers
Geslachten die in aanmerking komen voor studie
Beschrijving
Inclusion Criteria:
- Age ≥ 18 years
- Gender: Male/female
- h-Score probability ≥ 80%
- Known microbiological etiology
- Mild HLH not responding to infection specific targeted antimicrobial therapy (> 72 hours)
- Mild HLH developing new organ dysfunction
- Moderate to severe HLH with life threatening organ dysfunction
Exclusion Criteria:
- Primary (familial) HLH
- Malignancy associated HLH
- HLH associated with autoimmune disease
- EBV associated HLH
- Pregnancy
- Receiving immune modulator therapy within 2 moths
- Participants with HIV
- Consent not given
- Known hypersensitivity to IVIG or Dexamethasone
- Chronic liver disease
- Chronic kidney disease
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: Gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Geen (open label)
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
|
Actieve vergelijker: IVIg
Will receive intravenous Immunoglobulin (IVIg) therapy |
Injection IVIg (400 mg/kg Body weight) over an hour IV infusion X 5 days (total cumulative dose 2g/kg). Infection specific targeted antimicrobial therapy along with standard medical care |
|
Experimenteel: IVD
Will receive intravenous Dexamethasone (IVD) |
Infection specific targeted antimicrobial therapy along with standard medical care Injection Dexamethasone (10mg/m2) in 100 ml 0.9% normal saline (NS) over half an hour IV infusion X 3 days |
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Clinical remission
Tijdsspanne: 4 weeks
|
Number of participants become persistently asymptomatic without fever for ≥72 hours with h-Score probability <80% and without any HLH-related new organ dysfunction at 1 week and 4 weeks of the IVIG/IVD intervention |
4 weeks
|
|
The recovery of HLH-associated cytokines
Tijdsspanne: 4 weeks
|
Number of participants having reduction of HLH-associated cytokines (IL-1, IL-6, TNF-α, IFN-γ, GM-CSF) and Ferritin level from the pre-intervention baseline at 1 week and 4 weeks of the IVIG/IVD intervention |
4 weeks
|
Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Recovery of the hematological parameters
Tijdsspanne: 4 weeks
|
Number of participants with recovery or normalization of the hematological parameters (hemoglobin, total leukocyte count, and platelet count) |
4 weeks
|
|
Adverse events/ adverse drug reactions
Tijdsspanne: 4 weeks
|
Number of incidence of any adverse events and adverse drug reactions |
4 weeks
|
|
Duration of hospital stay
Tijdsspanne: 4 weeks
|
Number of days of hospital admission |
4 weeks
|
|
Incidence of relapse of HLH: Recurrence of HLH after achieving clinical remission
Tijdsspanne: 4 weeks
|
Number of participants having recurrence of HLH after achieving clinical remission |
4 weeks
|
Medewerkers en onderzoekers
Medewerkers
Onderzoekers
- Hoofdonderzoeker: Deba Prasad Dhibar, MD, Post Graduate Institute of Medical Education and Research, Chandigarh, India
Studie record data
Bestudeer belangrijke data
Studie start (Geschat)
Primaire voltooiing (Geschat)
Studie voltooiing (Geschat)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
- Lymfatische ziekten
- Histiocytose, niet-Langerhans-cel
- Histiocytose
- Hemische en lymfatische ziekten
- Lymfohistiocytose, hemofagocytose
- Health Services Administration
- Kwaliteit, toegang en evaluatie van de gezondheidszorg
- Aminozuren, peptiden en eiwitten
- Eiwitten
- Kwaliteit van de gezondheidszorg
- Kwaliteitsindicatoren, gezondheidszorg
- Enzymen
- Enzymen en co -enzymen
- Antilichamen
- Immunoglobulinen
- Immunoproteïnen
- Bloedeiwitten
- Serum -globulines
- Globulines
- Immunoglobuline -isotypes
- Immunoglobuline G
- Oxidoreductasen die werken op donoren van CH-CH-groep
- Oxidoreductasen
- Immunoglobulinen, intraveneus
- Zorgstandaard
- Therapeutica
- Isovaleryl-CoA-Dehydrogenase
Andere studie-ID-nummers
- PGI/IEC/2026/SPL-1447
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
Beschrijving IPD-plan
All the reasonable data requests should be submitted to the principal investigator (DPD) for consideration.
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
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