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rocuronium dosage for induction of general anesthesia is not associated with anaphylaxis severity: a retrospective study

rocuronium dosage for induction of general anesthesia is not associated with anaphylaxis severity: a retrospective study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500102482
Enrollment
Unknown
Registered
2025-05-15
Start date
2025-06-01
Completion date
Unknown
Last updated
2025-05-19

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

Conditions

Allergic reactions

Interventions

Perioperative anaphylactic shock (PAS) (experienced anaphylactic shock to rocuronium):None
Perioperative anaphylaxis(POA) (experienced anaphylactic tolerance to rocuronium):None

Sponsors

The First Affiliated Hospital of Zhengzhou University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Open to all genders; 2.Those who have undergone general anesthesia and have experienced anaphylactic shock or tolerance to rocuronium; 3.Those who exhibit a drop in blood pressure during the perioperative period, meeting the diagnostic criteria for a severe allergic reaction, with or without manifestations in other systems;

Exclusion criteria

Exclusion criteria: 1.Use of glucocorticoids during the perioperative period; 2.A drop in blood pressure during the perioperative period, with medical records indicating other confirmed causes of acute decompensation; 3.Individuals with incomplete medical records;

Design outcomes

Primary

MeasureTime frame
Plasma Histamine Level;Plasma Tryptase Level;The lowest value of mean arterial pressure;rocuronium dosage for induction of general anesthesia;Types, doses, and timing of perioperative medications;

Secondary

MeasureTime frame
Consumption of epinephrine;

Countries

China

Contacts

Public ContactZheng Qi

The First Affiliated Hospital of Zhengzhou University

15111510020@fudan.edu.cn+86 371 6976 7037

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026