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CLINICAL_TRIALS ClinicalTrials.gov record update

The Shwachman-Diamond Syndrome Global Patient Survey and Partnering Platform Program (SDS-GPS Program)

This page presents selected fields from the linked source record. It does not add a medical interpretation.

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT06999954
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-25T22:27:44.504171+00:00
Published At
2025-05-31T00:00:00+00:00
Record Updated At
2025-05-31
Timestamp Basis
source retrieval time was not retained by the feed adapter
Date limitation
source retrieval time was not retained by the feed adapter

Fields recorded by this source

protocolSection.conditionsModule.conditions
["Shwachman-Diamond Syndrome", "SDS", "IBMF", "Congenital Neutropenia", "Heme Malignancy", "Shwachman Syndrome", "Inherited Bone Marrow Failure", "Exocrine Pancreatic Insufficiency", "WHIM", "ELANE", "SBDS Gene Mutation", "EFL1 Gene Mutation", "DNAJC21 Gene Mutation", "SRP54 Gene Mutation", "Inherited Cancer Syndrome", "Inherited Cancer-Predisposing Syndrome", "Neutropenia, Severe Chronic", "Neutropenia Other", "Neutropenia Chronic Benign", "Ribosome Alteration", "Ribosomopathy", "Immune Deficiency", "Inherited BMF Syndrome", "Inherited Immunodeficiency Diseases", "Cognitive Delay, Mild", "Myelodysplastic Syndromes", "Pancytopenia"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2025-05-31"
protocolSection.identificationModule.nctId
"NCT06999954"
protocolSection.identificationModule.officialTitle
"The Shwachman-Diamond Syndrome Global Patient Survey and Partnering Platform Program (SDS-GPS Program)"
protocolSection.statusModule.overallStatus
"RECRUITING"
protocolSection.designModule.phases
[]
protocolSection.statusModule.resultsFirstPostDateStruct.date
""

Study condition terms

  • Shwachman-Diamond Syndrome (protocolSection.conditionsModule.conditions)
  • SDS (protocolSection.conditionsModule.conditions)
  • IBMF (protocolSection.conditionsModule.conditions)
  • Congenital Neutropenia (protocolSection.conditionsModule.conditions)
  • Heme Malignancy (protocolSection.conditionsModule.conditions)
  • Shwachman Syndrome (protocolSection.conditionsModule.conditions)
  • Inherited Bone Marrow Failure (protocolSection.conditionsModule.conditions)
  • Exocrine Pancreatic Insufficiency (protocolSection.conditionsModule.conditions)
  • WHIM (protocolSection.conditionsModule.conditions)
  • ELANE (protocolSection.conditionsModule.conditions)
  • SBDS Gene Mutation (protocolSection.conditionsModule.conditions)
  • EFL1 Gene Mutation (protocolSection.conditionsModule.conditions)
  • DNAJC21 Gene Mutation (protocolSection.conditionsModule.conditions)
  • SRP54 Gene Mutation (protocolSection.conditionsModule.conditions)
  • Inherited Cancer Syndrome (protocolSection.conditionsModule.conditions)
  • Inherited Cancer-Predisposing Syndrome (protocolSection.conditionsModule.conditions)
  • Neutropenia, Severe Chronic (protocolSection.conditionsModule.conditions)
  • Neutropenia Other (protocolSection.conditionsModule.conditions)
  • Neutropenia Chronic Benign (protocolSection.conditionsModule.conditions)
  • Ribosome Alteration (protocolSection.conditionsModule.conditions)
  • Ribosomopathy (protocolSection.conditionsModule.conditions)
  • Immune Deficiency (protocolSection.conditionsModule.conditions)
  • Inherited BMF Syndrome (protocolSection.conditionsModule.conditions)
  • Inherited Immunodeficiency Diseases (protocolSection.conditionsModule.conditions)
  • Cognitive Delay, Mild (protocolSection.conditionsModule.conditions)
  • Myelodysplastic Syndromes (protocolSection.conditionsModule.conditions)
  • Pancytopenia (protocolSection.conditionsModule.conditions)

Intervention details are not present in the imported fields for this record. No drug-condition relationship is inferred from co-listing.

This index keeps the source fields it imported; it may not contain the complete original record. Verify wording and context in the linked source.