Brief Title
Impact of Pain on Functional Impairment and Quality of Life in Adults With Hemophilia
Official Title
Impact of Pain on Functional Impairment and Quality of Life in Adults With Hemophilia
Brief Summary
This study is conducted in the United States of America (USA). The aim of the study is to assess the impact of pain on functional impairment and quality of life in adult persons with hemophilia (PWH) with and without inhibitors with joint bleeding.
Study Type
Observational
Primary Outcome
Prevalence of acute (bleed-related) pain (percentage)
Condition
Congenital Bleeding Disorder
Intervention
No treatment given
Study Arms / Comparison Groups
Adult PWH
Description:
Publications
* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
Recruitment Information
Recruitment Status
Other
Estimated Enrollment
381
Start Date
October 2013
Completion Date
October 2014
Primary Completion Date
October 2014
Eligibility Criteria
Inclusion Criteria: - Adult males able to provide consent and complete a survey in English - Congenital hemophilia A or B with or without inhibitors with any history of joint bleeding or joint pain - Presentation at the treatment center for a comprehensive annual visit where joint range of motion will be obtained - Informed consent obtained before any study-related activities. (Study-related activities are any procedure related to recording of data according to the protocol) Exclusion Criteria: - Previous participation in this study
Gender
Male
Ages
N/A - N/A
Accepts Healthy Volunteers
No
Contacts
Global Clinical Registry (GCR, 1452), ,
Location Countries
United States
Location Countries
United States
Administrative Informations
NCT ID
NCT01988532
Organization ID
HAEM-4073
Secondary IDs
U1111-1138-3464
Responsible Party
Sponsor
Study Sponsor
Novo Nordisk A/S
Study Sponsor
Global Clinical Registry (GCR, 1452), Study Director, Novo Nordisk A/S
Verification Date
January 2017