Survey Evaluating the Psychosocial Effects of Living With Haemophilia

NCT01322620 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1236

Last updated 2017-02-23

No results posted yet for this study

Summary

This study is conducted in Africa, Asia, Europe, North America and South America.

The purpose of the survey is to identify the key psychosocial issues affecting patients with haemophilia.

Conditions

  • Congenital Bleeding Disorder
  • Haemophilia A
  • Haemophilia B
  • Haemophilia A With Inhibitors
  • Haemophilia B With Inhibitors
  • Relatives to/Carers of Patients

Interventions

OTHER

No treatment given

No treatment given. Participants are to complete a questionnarie in the study.

Sponsors & Collaborators

Principal Investigators

  • Global Clinical Registry (GCR, 1452) · Novo Nordisk A/S

Eligibility

Min Age
18 Years
Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-06-03
Primary Completion
2012-02-29
Completion
2012-02-29

Countries

  • Canada
  • Spain
  • United Kingdom

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01322620 on ClinicalTrials.gov