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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01029808
Other study ID # VGAO002
Secondary ID
Status Completed
Phase N/A
First received December 9, 2009
Last updated October 18, 2016
Start date December 2009
Est. completion date July 2011

Study information

Verified date October 2016
Source Sahlgrenska University Hospital, Sweden
Contact n/a
Is FDA regulated No
Health authority Sweden: Regional Ethical Review Board
Study type Observational

Clinical Trial Summary

To collect and analyze data on female carriers of severe and moderate hemophilia A and B.


Recruitment information / eligibility

Status Completed
Enrollment 126
Est. completion date July 2011
Est. primary completion date July 2011
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Female carriers of hemophilia A and B.

Exclusion Criteria:

- Pregnancy.

Study Design

Observational Model: Cohort, Time Perspective: Cross-Sectional


Related Conditions & MeSH terms


Locations

Country Name City State
Sweden Sahlgrenska university hospital Göteborg

Sponsors (1)

Lead Sponsor Collaborator
Sahlgrenska University Hospital, Sweden

Country where clinical trial is conducted

Sweden, 

References & Publications (2)

Olsson A, Hellgren M, Berntorp E, Baghaei F. Association between bleeding tendency and health-related quality of life in carriers of moderate and severe haemophilia. Haemophilia. 2015 Nov;21(6):742-6. doi: 10.1111/hae.12796. Epub 2015 Sep 8. — View Citation

Olsson A, Hellgren M, Berntorp E, Ljung R, Baghaei F. Clotting factor level is not a good predictor of bleeding in carriers of haemophilia A and B. Blood Coagul Fibrinolysis. 2014 Jul;25(5):471-5. doi: 10.1097/MBC.0000000000000083. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Bleeding tendency in carriers of severe and moderate haemophilia compared to a control group. Five years No
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