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Trial · NCT07410130

Clinical Spectrum and Management of Von Willebrand Disease Among Children in Assiut Governorate

NCT07410130, Not yet recruiting, Assiut University

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Clinical Spectrum and Management of Von Willebrand Disease Among Children in Assiut Governorate. Trials, record NCT07410130. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07410130

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Clinical Spectrum and Management of Von Willebrand Disease Among Children in Assiut Governorate
NCT number
NCT07410130
Status
Not yet recruiting
Enrollment
25 participants, estimated
Lead sponsor
Assiut University
Conditions
Von Willebrand Disease (VWD), Inherited Bleeding Disorders in Children, Pediatric Hemostatic Disorders
Interventions
Tranexamic Acid, Von Willebrand Factor-Containing Concentrates
First posted
2026-02-13
Last updated
2026-02-13

Source ClinicalTrials.gov

Registered outcomes6

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryFrequency of Von Willebrand Disease Among Investigated Childrenat enrollmentThe proportion of children diagnosed with von Willebrand disease among those evaluated for suspected bleeding disorders at Assiut University Children's Hospital.
PrimaryDistribution of Von Willebrand Disease SubtypesWithin 2 weeks of enrollmentClassification and relative frequency of von Willebrand disease types (Type 1, Type 2, and Type 3) according to ISTH diagnostic criteria based on laboratory findings.
PrimaryClinical Bleeding Patterns in Children With Von Willebrand Diseaseat enrollment.Assessment of bleeding manifestations, including epistaxis, bruising, mucosal bleeding, postsurgical bleeding, and menorrhagia, using standardized clinical evaluation and bleeding assessment tools.
OtherUse of Von Willebrand Factor-Containing ConcentratesFrom enrollment up to 6 months of follow-upFrequency of administration of VWF-containing concentrates during bleeding episodes or as prophylaxis.
OtherHealthcare utilizationUp to 6 months following enrollmentNumber of emergency department visits or hospital admissions related to bleeding episodes during the follow-up period.
OtherAdverse Events Related to TreatmentFrom enrollment up to 6 months of follow-upOccurrence of treatment-related adverse events, including allergic reactions or other reported complications.

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers7

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
454454BACKGROUNDPubMed
20307244BACKGROUNDPubMed
21301780BACKGROUNDPubMed
26375306BACKGROUNDPubMed
31612544BACKGROUNDPubMed
31808831BACKGROUNDPubMed
32573918BACKGROUNDPubMed

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT07410130

GET https://conductscience.org/api/trials/v1/NCT07410130/registered