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Evaluation of the Efficiency of Hydration by Isotonic Solution in the Prevent of the Fainting Whole Blood Donors

Evaluation of the Efficiency of a Hydration by Isotonic Solution With or Without Muscular Exercise of the Fainting Whole Blood Donors

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02075099
Acronym
EVASION
Enrollment
4825
Registered
2014-03-03
Start date
2014-01-31
Completion date
2014-08-31
Last updated
2015-02-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Fainting, Presyncope, Syncopal Episode

Keywords

whole blood donation, donation water drink, isotonic drink, presyncopal and syncopal reactions

Brief summary

Blood donation is a generous act carried out by healthy male and female volunteer donors. The safety of blood donation in France is based on rigorous well documented biological and medical criteria, in particular concerning the volume of blood to be taken. While whole blood donation is very safe, some donors experience faintness during or after donation. Any injury resulting from a fall increases its seriousness, especially when it happens outside the donation site. According to various studies, adverse reactions are experienced by between 0.28% and 2.72% of all donors and occur in all categories (sex and age). A retrospective evaluation of the frequency of faintness incidents on during whole blood donation over 2012 in the Rhone Alpes' region of France shows a frequency ranging from 1.05% in mobile donation units in towns to 4.24% in donation units in high schools, with no reporting of delayed incidents of faintness by this donor population.

Detailed description

Despite precautions including advice to donors to drink some water before blood donation, fainting events still occur. They can have an impact on the frequency of donation as well as on the blood donor's motivation and that in their close entourage. This impact should not be overlooked in the context of the increasing need for blood components and tighter budgets.. In some other national health systems, the donor is given a drink shortly before giving blood and / or donors are advised to do lower-body muscle tensing exercises whilst giving blood. The present study has a factorial design and compares 3 arms for hydration criteria and 2 arms for exercise criteria with cluster randomization (1 cluster = 1 blood donation unit). The randomization plan will be stratified according to the type of EFS donation unit (French Blood Donation service: Etablissement Français du Sang): Fixed/Mobile unit; and also on the location of the of mobile blood donation unit: in companies, towns or schools. In the latter, the blood donors have a potentially higher risk of presyncopal or syncopal reactions. 3 arms: * 500mL of an isotonic drink to be drunk immediately before blood donation * 500mL of slightly mineralized water to be drunk immediately before blood donation * Advice to drink one glass of fruit juice or water before blood donation In the 3 arms, the centralized randomization will balance the numbers of blood donations in which the donors will perform lower-body muscle tensing exercises , or not, during the blood donation. Main objective: To assess the impact of preventive measures, including rapid hydration with 500mL of an isotonic drink versus hydration with 500mL of water or simple advice to have a drink; and advice to perform lower-body muscle tensing exercises during the whole blood donation, on the prevention of presyncopal and syncopal reactions during blood donation and in the following 48 hours.

Interventions

OTHERtensing exercises

Donors will do tensing exercises during blood donation

OTHERNo tensing exercises

Donors will not do tensing exercises during blood donation - control arm

Sponsors

University Hospital, Grenoble
CollaboratorOTHER
Etablissement Français du Sang
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 71 Years
Healthy volunteers
Yes

Inclusion criteria

\- Whole blood donors , in fixed site or mobile collection * 18-year-old and less than 71 years * Donor with weight \> in 50 kg and height\> 135 cms * Whole Blood donors having had an interview with a doctor of the EFS and declared capable * Donors for phone contact in 7 days following the donation

Exclusion criteria

* Collection by an autonomous mobile blood collection unit (with independent management and sample storage) * Donor with an immobilization, even partial, of a lower limb. * Donor allergic to shellfish, gluten, milk or soya. * Donor under judicial protection or other administrative control.

Design outcomes

Primary

MeasureTime frameDescription
Accumulated incidence of presyncopal and syncopal reactions during blood donation, while still at the blood donation whole and within 48 hours of the blood donation, that required the donor to be placed in a 'Trendelenburg' positionAt the time of inclusion and at 48 hours after the blood donationSymptoms of presyncopal reactions (blurring of vision, insensitivity to ambient noises, generalized weakness, paleness, nausea) and syncopal reactions that required the donor to be placed in the 'Trendelenburg' position * Presyncopal and syncopal symptoms requiring interruption of the blood donation * Vomiting * Unconsciousness with interruption of blood donation, with no other consequences and no specific treatment. * Convulsions * Leak of urine * Unconsciousness with interruption of blood donation with no other consequences, but with medical treatment by an oral route. * Unconsciousness with interruption of blood donation with no other consequences, but requiring a perfusion or intravenous treatment. * Unconsciousness immediately post donation with or without consequences * Presyncopal and syncopal reactions with or without consequences within the 48 hours after the blood donation * Angina, infarct * Death

Secondary

MeasureTime frameDescription
presyncopal and syncopal reactions of all donorsinclusion and 48 hours after the blood donationThis concerns presyncopal and syncopal reactions that required the donor to lie down in the Trendelenburg position and any further intervention. We will compare the occurrence of presyncopal and syncopal reactions during the blood donation, or immediately post-donation, while still in the blood donation center, and within 48 hours following blood donation. We will analysed separate from that of the main criterion in three periods: during the donation, immediate post donation, late post donation.
presyncopal and syncopal reactions in the population of young donors (in schools)48 hours after the blood donationMain criteria analyzed in the sub-population of blood donation at schools Evaluate the rate of presyncopal and syncopal reactions after the donation, but within 48 hours, in the population of young donors attending blood collection centers in schools.
presyncopal or syncopal reactions influence on subsequent blood donationyear which follows the blood donationEvaluate the influence of the occurrence of presyncopal or syncopal reactions on subsequent blood donation or not. Renewal of blood donation within one year (from the EFS database)
Recurrence of presyncopal or syncopal reactionsyear which follows the blood donationPresyncopal and syncopal reactions during a following blood donation made within one year and listed in the EFS donor safety database Evaluate whether the occurrence of presyncopal or syncopal reactions is a predictor of recurrence during the next blood donation
daily activities48 hours after the blood donationEvaluation of the impact of whole blood donation assess by : Modification of daily habits. Fatigue assessment scale for healthy subjects. Unusual fatigue depending on the type of proposed prevention (drinks and exercises).
subgroup analysis on collection unit characteristics7 days after last donor inclusionsubgroup analyses of the primary and secondary endpoints according to the characteristics of the collection unit used in the stratification of randomization of donors.
medium term impact of the donation7 days after the blood donationMain criterion and secondary criteria assessed at day 7 by phone call to the donor
Restless legs syndromemonths before the blood donationduring phone call to the donor at day 7, questions will be asked about possible or probable RLS (Restless Legs Syndrome). Classification of Bryan R. Spencer (Transfusion August 2013) will be used.
Explanatory variables of presyncopal and syncopal reactions7 days after last donor inclusionVariables linked to the presyncopal and syncopal reactions as defined by the main criterion Explanatory variables: the characteristics of the donor (age, sex, number of previous blood donations), the circumstances of the blood donation (work or effort before the blood donation, the time of day of the blood donation, the quality of the post donation snack (sweet/salty) etc. and the characteristics of the blood donation unit/center (fixed/mobile, school/company/town, room/ mobile blood donation unit, size of the town, place of blood donation.

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026