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Clinical Trials/ISRCTN24760606
ISRCTN24760606
Active, not recruiting
未知

A randomised trial to determine whether the interval between blood donations in England can be safely and acceptably decreased

HS Blood and Transplant (NHSBT) (UK)0 sites50,000 target enrollmentJanuary 25, 2012
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ConditionsOptimum intervals for blood donationNot Applicable

Overview

Phase
未知
Intervention
Not specified
Conditions
Optimum intervals for blood donation
Sponsor
HS Blood and Transplant (NHSBT) (UK)
Enrollment
50000
Status
Active, not recruiting
Last Updated
6 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

2014 protocol in: https://www.ncbi.nlm.nih.gov/pubmed/25230735 2016 results in: https://www.ncbi.nlm.nih.gov/pubmed/27645285 2017 results in: https://www.ncbi.nlm.nih.gov/pubmed/28941948 2019 extension study results in: https://www.ncbi.nlm.nih.gov/pubmed/31383583 (added 07/08/2019)

Registry
who.int
Start Date
January 25, 2012
End Date
November 1, 2021
Last Updated
6 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
HS Blood and Transplant (NHSBT) (UK)

Eligibility Criteria

Inclusion Criteria

  • •1\. Age \>17 years and fulfilling all normal criteria for blood donation
  • •2\. Willing to be assigned to any of the study intervention groups
  • •3\. Registered at one of the permanent donation clinics at the time of enrolment

Exclusion Criteria

  • •Current exclusion criteria as of 22/05/2012:
  • •1\. As the aim of the study is to be almost ?paper\-less?, it will involve remote web\-based data collection. Hence, participants who do not have internet access and/or are not willing to provide an email address for study correspondence will be excluded
  • •Previous exclusion criteria:
  • •1\. Donors who are providing extra samples to NHSBT at their initial visit (e.g. for the British bone marrow registry) as there will be insufficient blood left in the sample pouch for the collection of study samples
  • •2\. As the aim of the study is to be almost ?paper\-less?, it will involve remote web\-based data collection. Hence, participants who do not have internet access and/or are not willing to provide an email address for study correspondence will be excluded
  • •3\. Donors who have been identified for ?special panels? by NHSBT

Outcomes

Primary Outcomes

Not specified

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