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PenDel: Penicillin Allergy Delabeling Among Surgical Patients

Sponsor
University Medicine Greifswald (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05956080
Collaborator
(none)
600
Enrollment
1
Arm
24
Anticipated Duration (Months)

Study Details

Study Description

Brief Summary

Penicillin allergy testing among surgical patients

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Allergy testing
 N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
600 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Penicillin Allergy Delabeling Among Surgical Patients
Anticipated Study Start Date :
Sep 1, 2023
Anticipated Primary Completion Date :
Sep 1, 2025
Anticipated Study Completion Date :
Sep 1, 2025

Arms and Interventions

Arm Intervention/Treatment
Other: Allergy testing

Diagnostic Test: Allergy testing
University Medicine Greifswald

Outcome Measures

Primary Outcome Measures

  1. Confirmed penicillin allergy [1 week]

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • surgical patients with reported penicillin allergy
Exclusion Criteria:
  • missing consent

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • University Medicine Greifswald

Investigators

  • Principal Investigator: Sebastian Gibb, MD, University Medicine Greifswald
  • Principal Investigator: Christian S. Scheer, MD, University Medicine Greifswald

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University Medicine Greifswald
ClinicalTrials.gov Identifier:
NCT05956080
Other Study ID Numbers:
  • 003
First Posted:
Jul 21, 2023
Last Update Posted:
Jul 21, 2023
Last Verified:
Jul 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:
Hypersensitivity
Drug Hypersensitivity

Study Results

No Results Posted as of Jul 21, 2023