Trials / Completed
CompletedNCT03804346
Infantile - Postoperative Residual Curarization - Study
Observational Study to Detect Postoperative Residual Curarization in Infantile Patients
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 100 (actual)
- Sponsor
- University of Regensburg · Academic / Other
- Sex
- All
- Age
- 1 Month – 18 Years
- Healthy volunteers
- Accepted
Summary
The primary object of this study is, to investigate the current procedure of neuromuscular monitoring at a tertiary academic university medical center.
Detailed description
Residual neuromuscular block is known to be a significant but frequently overlooked complication after the use of neuromuscular blocking agents. Aim of this prospective, observational study is to detect the incidence and severity of residual paralysis at a tertiary academic german university medical center. Methods: All infantile patients recieving neuromuscular blocking agents are included over a 12 week observational period. At the end of the operation procedure, directly prior to tracheal extubation a train-of-four ratio was assessed quantitatively by an independet observer using the TOF Watch SX monitor. Data related to patient postoperative outcome were collected in the operating theatre, during the way to the postoperative care unit (PACU) and during the stay in the PACU: * incidence of residual paralysis * incidence of aspiration, bronchospasm, laryngospasm, oxygen desaturation, airway obstruction,
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DIAGNOSTIC_TEST | Acceleromyography | At the End of Surgery, shortly before Extubation, the TOF-Ratio is measured by an independent investigator using Acceleromyography. |
Timeline
- Start date
- 2017-05-01
- Primary completion
- 2017-07-23
- Completion
- 2017-07-23
- First posted
- 2019-01-15
- Last updated
- 2019-01-15
Locations
1 site across 1 country: Germany
Source: ClinicalTrials.gov record NCT03804346. Inclusion in this directory is not an endorsement.