RecruitingNot ApplicableNCT06803758

Teicoplanin Allergy Testing Using Autologous Serum (TATAS)

Improving The Sensitivity of Teicoplanin Allergy Testing By Using Autologous Serum


Sponsor

University Hospital Southampton NHS Foundation Trust

Enrollment

20 participants

Start Date

Jan 8, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

Allergy testing for Teicoplanin is much more unreliable than for other similar drugs. This means that we run the risk of missing serious Teicoplanin allergy, and these patients will be given another dose in future, not knowing that they are seriously allergic. Serious allergic reactions, also known as anaphylaxis, can be life threatening. The patients which we recruit to our study will come to us through the perioperative allergy service. They will have had a reaction to a general anaesthetic, but will also have had teicoplanin as part of the anaesthetic. We are not sure why allergy skin testing, which is fairly reliable for most other drugs, is so unreliable in detecting teicoplanin allergy. We do know that some drugs need to mix with proteins in the blood before they trigger an allergy. We would like to replicate this by mixing the teicoplanin with the patients' own blood and using this for the skin testing, to see if we get a more reliable result compared with the plain drug. Using the patient's own serum to do skin testing is an established test (the 'autologous serum test') used in certain immunological conditions, we are simply going to use it as a vehicle to test our theory. We will recruit 20 adult patients referred with a recent history of anaphylaxis under anaesthesia, where teicoplanin has been given and is one of the drugs under suspicion of having caused the allergy. In addition to the usual allergy skin testing, which would be done anyway as part of standard allergy investigation, we will perform extra tests using autologous serum for this trial. We hope to find a better way of testing for Teicoplanin allergy, so that patients are not put at risk where the allergy has been missed because of an unreliable test.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study investigates whether a new skin testing method using a patient's own blood serum mixed with teicoplanin (an antibiotic) can more accurately detect teicoplanin allergy compared to standard skin tests, which are known to be unreliable for this particular drug. Teicoplanin is sometimes given during surgery, and missing a true allergy could put future patients at risk of a life-threatening allergic reaction (anaphylaxis). Adults aged 18 or older who experienced a suspected anaphylaxis reaction during anesthesia where teicoplanin was one of the drugs given are eligible. Participation involves attending an allergy clinic for additional skin tests using your own serum alongside routine allergy testing — no extra invasive procedures beyond what would normally be done. This summary was generated by AI to help patients understand the study in plain language.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DIAGNOSTIC_TESTTeicoplanin Allergy Testing using autologous serum

In addition to performing teicoplanin allergy skin testing using standard recommended Teicoplanin concentration, we will perform skin testing using autologous serum, the supernatant which is obtained via centrifugation. Skin testing ( skin prick test and intradermal test) will be performed with these additional samples: 1. STpre: Teicoplanin added to blood sample pre-centrigufation. 2. STpost: Teicoplanin added to supernatant post-centrigufation. 3. ST0: Supernatant with no additives ( serum negative control)


Locations(1)

University Hospital Southampton

Southampton, United Kingdom

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NCT06803758


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