ClinicalTrials.gg
Status unknownNCT04825158HEMOCANOPEUpdated Apr 1, 2021

Study of the Role of Hemostasis in Perioperative Anaphylaxis

An observational study in Hemoptysis, Perioperative Complication and Anaphylaxis, sponsored by University Hospital, Strasbourg, France. Status unknown. Open to participants aged 2 Years and older. Per ClinicalTrials.gov, last updated 2021-04-01.

Sponsored by University Hospital, Strasbourg, France · Observational

The sponsor has not verified this record recently (last verified Mar 2021), so the status shown — last known as Not yet recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
30
Ages
2 Years and older
Sex
All
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Study summary

Anaphylaxis is a severe and life-threatening complication during the perioperative period. Perioperative anaphylaxis is still associated with a significant mortality despite quick and efficient management using epinephrine, the mainstay of acute treatment. Experimental data and few case reports are suggesting that hemostasis, and more precisely platelets, could play a role in anaphylaxis. Our main hypothesis is that activation of the hemostatic system contributes to the severity of the reaction

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Conditions studied

  • Hemoptysis
  • Perioperative Complication
  • Anaphylaxis
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In context

Hemoptysis

37 studies on the registry are indexed under Hemoptysis; 6 are open to participants now.

This study's planned enrollment of 30 is below the median of 176 across 15 observational studies indexed under Hemoptysis.

Browse Hemoptysis studies →

Lead sponsor

University Hospital, Strasbourg, France is the lead sponsor of 999 studies on the registry; 358 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
2 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

The study will focus on any adult patient with a suspected diagnosis of perioperative anaphylactic shock

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Patient, male or female, adult
  • In the perioperative period
  • In whom the diagnosis of anaphylactic shock is suggested
  • Patient is giving his consent to participate in the study

Exclusion criteria

Exclusion Criteria:

  • Subject under legal protection
  • Subject under guardianship or guardianship
  • Anemia less than 7 g /dl at the time of inclusion
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
30 participants (estimated)
Patient registry
No
Biospecimen retention
Samples without dna
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What researchers measure

Primary outcomes

  1. Platelet activation

    Measurement of: Plasmatic serotonin level, Plasmatic PF-4 level, P-selectin expression (MFI, %), Platelet count

    Time frame: As soon as possible after onset of anaphylaxis

  2. Platelet activation

    Measurement of: Plasmatic serotonin level, Plasmatic PF-4 level, P-selectin expression (MFI, %), Platelet count

    Time frame: 1-2 hours after the onset of anaphylaxis

  3. Platelet activation

    Measurement of: Plasmatic serotonin level, Plasmatic PF-4 level, P-selectin expression (MFI, %), Platelet count

    Time frame: 24 hours after the onset of anaphylaxis

  4. Platelet activation

    Measurement of: Plasmatic serotonin level, Plasmatic PF-4 level, P-selectin expression (MFI, %), Platelet count

    Time frame: During the allergic workup (4-6 weeks after)

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Study locations

No study locations are listed for this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 1, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04825158
Responsible party
Sponsor
First posted
Apr 1, 2021
Start date
Apr 1, 2021 (estimated)
Primary completion
Apr 1, 2021 (estimated)
Completion
Feb 9, 2024 (estimated)
Last update
Apr 1, 2021

Study contacts

Charles-Ambroise TACQUARD, PHD
Contact
charlesambroise.tacquard@chru-strasbourg.fr
+333 69 55 16 08
Xavier DELABRANCHE, PHD
Contact
Xavier.delabranche@chru-strasbourg.fr
03.69.55.09.36

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Mar 2021. You cannot join it, but the record below documents what was studied.

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