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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03915873
Other study ID # BS in VWD
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date December 1, 2019
Est. completion date March 1, 2021

Study information

Verified date September 2019
Source Assiut University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Applying the ISTH-BAT questionnaire on Egyptian patients with type I VWD aiming to correlate the BS with the laboratory findings


Description:

The clinical phenotype of the disease is variable and tends to be mild in type 1 vWD, whereas it shows serious bleeding manifestations in types 2 and 3. Overall, the symptoms reported in vWD include easy bruising, epistaxis, gastrointestinal bleeding, excessive menstrual bleeding, postpartum haemorrhage, and excessive bleeding after surgical operation and minor wounds.However, A distinctive bleeding history is a prerequisite for the diagnosis of any bleeding disorder and should guide further laboratory investigations In an attempt to standardize the diagnostic criteria of VWD, a bleeding questionnaire and a bleeding score were developed The combination of a standardized bleeding questionnaire and a well-defined interpretation grid (for the computation of the final (BS) has been referred to as a Bleeding Assessment Tool (BAT).


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 20
Est. completion date March 1, 2021
Est. primary completion date December 1, 2020
Accepts healthy volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- type 1 vWD patients

- healthy subjects with no known problem with bleeding or bruising were also recruited

Exclusion Criteria:

-

Study Design


Intervention

Diagnostic Test:
The von Willebrand Antigen level
blood sample

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Assiut University

Outcome

Type Measure Description Time frame Safety issue
Primary the International Society on Thrombosis and Hemostasis-Bleeding Assessment Tool (ISTH-BAT) Questionnaire minimum score ranges from 0 to 10 whereas maximum score ranges from 20 to 30 one year
See also
  Status Clinical Trial Phase
Recruiting NCT06064851 - Delivering Transcutaneous Auricular Neurostimulation to Reduce Heavy Menstrual Bleeding in Von Willebrand Disease Patients N/A