# Standardised Drug Provocation Testing in Perioperative Hypersensitivity

> **NCT06065137** · NA · COMPLETED · sponsor: **University Hospital, Antwerp** · enrollment: 50 (actual)

## Conditions studied

- Allergic Reaction
- Hypersensitivity
- Perioperative Complication
- Anaphylaxis
- Anaphylactic Reaction
- Immediate Hypersensitivity
- Hypersensitivity, Drug

## Interventions

- **DIAGNOSTIC_TEST:** Full dose DPT with propofol
- **DIAGNOSTIC_TEST:** Full dose DPT with ketamine
- **DIAGNOSTIC_TEST:** Full dose DPT with etomidate
- **DIAGNOSTIC_TEST:** Full dose DPT with midazolam
- **DIAGNOSTIC_TEST:** Full dose DPT with fentanyl
- **DIAGNOSTIC_TEST:** Full dose DPT with sufentanyl
- **DIAGNOSTIC_TEST:** Full dose DPT with alfentanil
- **DIAGNOSTIC_TEST:** Full dose DPT with remifentanil
- **DIAGNOSTIC_TEST:** Full dose DPT with rocuronium
- **DIAGNOSTIC_TEST:** Full dose DPT with atracurium
- **DIAGNOSTIC_TEST:** Full dose DPT with cisatracurium
- **DIAGNOSTIC_TEST:** Full dose DPT with succinylcholine

## Key facts

- **NCT ID:** NCT06065137
- **Lead sponsor:** University Hospital, Antwerp
- **Sponsor class:** OTHER
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2023-10-23
- **Primary completion:** 2025-06-30
- **Final completion:** 2025-06-30
- **Target enrollment:** 50 (ACTUAL)
- **Last updated:** 2025-09-08


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT06065137

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT06065137, "Standardised Drug Provocation Testing in Perioperative Hypersensitivity". Retrieved via AI Analytics 2026-06-25 from https://api.ai-analytics.org/clinical/NCT06065137. Licensed CC0.

---

*[Clinical trials dataset](/datasets/clinical-trials) · CC0 1.0*