Comparison of the response observed in the dominant and non-dominant hands when assessing neuromuscular block using the TOF-Watch® SX

Not Applicable

Completed

• Conditions: Routine surgery/neuromuscular block; Surgery; Routine surgery

• Registration Number: ISRCTN82219498
• Lead Sponsor: Belfast Health and Social Care Trust (UK)

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2009-10-14
• Last Update Posted: 3 April 2017

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

1. American Society of Anaesthesiologists (ASA) grade I - III
2. Aged 18 - 65 years, either sex
3. Undergoing planned, elective surgery

Exclusion Criteria

1. Patients with known neuromuscular disease
2. Patients on medication known to interact with neuromuscular blocking agents
3. Pregnancy
4. Patients with known allergy to neuromuscular blocking agents
5. Patients with a known or suspected risk of difficult intubation

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Time to return of TOF (train-of-four) ratio to 0.9

Secondary Outcome Measures

Name	Time	Method
1. Tme to onset of block<br>2. Time to return of T1 to 25%