Observational Study to see the process of recovery from Anaesthesia while monitoring muscle contraction using Neuromuscular monitoring system
Not Applicable
Completed
- Conditions
- Health Condition 1: null- patients posted for general surgical proceudres of less than 2 hours duration under general anaeshtesia.
- Registration Number
- CTRI/2017/06/008841
- Lead Sponsor
- RESEARCH CE
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 200
Inclusion Criteria
The primary outcome of the study was the time required to achieve TOF ratio of 0.9 at the end of surgery, without giving neostigmine while extubating the patients at TOF ratio of 0.9.
Exclusion Criteria
1) The patients with history of diabetes, myasthenia gravis.
2) The patients with hepato-renal impairment.
3) Patients having surgery at the site where electrodes were to be applied
4) All types of emergency surgeries.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcome of the study was the time required to achieve TOF ratio of 0.9 at the end of surgery, without giving neostigmine and extubating the patients at TOF ratio of 0.9.Timepoint: TOF ratio of 0.9
- Secondary Outcome Measures
Name Time Method The secondary outcome measures were incidence of post-operative residual curarization (PORC) in post anaesthesia care unit (PACU) when neostigmine was not given for reversal, incidence of reintubation in PACU, incidence of nausea, vomiting in PACU and time required to shift the patients from PACU to wards, when neostigmine is not used for reversing NMB at the end of surgery.Timepoint: PACU: 0 to 2 hrs