Overview

A Comparison of Rocuronium 0.3 mg/kg, and 0.9 mg/kg for Induction of Anesthesia in Elderly Patients.

Status:
Completed
Trial end date:
2021-05-25
Target enrollment:
0
Participant gender:
All
Summary
The number of elderly patients above 80 years is increasing and a large proportion of these patients will require surgery and anesthesia. During anesthesia neuromuscular blocking agents (NMBA) are administered to facilitate intubating conditions and reduce the trauma to the larynx and vocal cords. There is a risk of residual neuromuscular block when using NMBAs like rocuronium. The aim of this study is to determine the onset time, duration of action and effect on intubating conditions after rocuronium 0.3 mg/kg and 0.9 mg/kg in patients with age ≥ 80 years.
Phase:
N/A
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Rigshospitalet, Denmark
Treatments:
Rocuronium
Criteria
Inclusion Criteria:

- Age ≥ 80

- Scheduled to elective surgery (expected duration time of surgery > 1 hour) under
general anesthesia with intubation and use of rocuronium.

- American Society of Anesthesiologists (ASA) physical status classification I to III

- Informed consent (see appendix 1)

- Read and understand Danish

Exclusion Criteria:

- Neuromuscular disease

- Known allergy to rocuronium

- Prone position

- Indication for rapid sequence induction