Neuromuscular Blockade Clinical Trial
Official title:
Anaesthesia With or Without Neuromuscular Blocking Agents in Intubation and Intraoperative Nerve-monitoring During Thyroid Surgery: a Feasibility and Safety Pilot Study.
NCT number | NCT03910504 |
Other study ID # | IONM |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | April 17, 2019 |
Est. completion date | December 30, 2019 |
Verified date | November 2020 |
Source | University Magna Graecia |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
In this randomized controlled trial the investigators want to assess if, compared to controls, the administration of one single low-dose of rocuronium would increase the occurrence of absent or weak (i.e. amplitude <100 μV) signal at V1 and R1, indicating a residual NMBA activity. In addition, we also recorded: 1) the occurrence of difficult laryngoscopy; 2) the time-to-intubation; 3) the occurrence of difficult intubation; 4) the number of intubation attempts; 5) the intubation failure rate; 6) the need for oxygenation between intubation attempts; 7) the lowest peripheral saturation in oxygen (SpO2); 8) the number of severe desaturations; 9) the time-to-V1 and 10) the number of post-surgical complications.
Status | Completed |
Enrollment | 100 |
Est. completion date | December 30, 2019 |
Est. primary completion date | December 30, 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Elective surgery of the thyroid with the use of Intra-Operative Neuromuscular Monitoring (IONM) Exclusion Criteria: - Patients who suffer from paralysis of vocal cords or diseases of neuromuscular system. - Patients with a history of allergy to anaesthetic drugs. - Patients who has a high possibility of difficult intubation due to one the following criteria: a) interdental distance < 20 mm; b) marked upper teeth protrusion (mandibular prognathism), which is not possible to correct; c) thyromental distance = 60 mm; d) Mallampati class 4; e) macroglossia with marked micrognathia; f) fixed neck flection; g) severe scar tissue or post radiation fibrosis of the tongue. - Patients who has a high possibility of difficult intubation due to two of the following criteria, associated with each other: a) interdental distance < 35 mm; b) moderate prognathism or retrgnathia; c) mentohyoid distance < 40 mm; d) thyromental distance = 65 mm; e) Mallampati class 2-3; f) reduced head-neck flexion and extension; g) Body Mass Index (BMI) > 30 kg/m2. |
Country | Name | City | State |
---|---|---|---|
Italy | AOU Mater Domini | Catanzaro |
Lead Sponsor | Collaborator |
---|---|
Federico Longhini |
Italy,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Occurrence of absent or weak signal at V1 and R1 (i.e. amplitude <100 µV) | Record of the vagus (V1) and recurrent laryngeal nerve (R1) with the intraoperative neuromuscular monitoring before the dissection of the thyroid | Immediately after vagus and recurrent laryngeal nerve identification | |
Secondary | Time of intubation | The time of intubation is intended as the duration from the moment when the anaesthesiologist takes the laryngoscope till the first end-tidal carbon dioxide record | Immediately after successful endotrachel intubation | |
Secondary | Rate of difficult intubation | Difficult orotracheal intubation is defined as an intubation, which requires more than 2 laryngoscopies, which continues more than 10 minutes, or whether it claims the use of alternative devices | Immediately after successful endotrachel intubation | |
Secondary | Cormack Lehane scale value | Evaluation of laryngeal exposition according to Cormack-Lehane (1: Full view of glottis; 2a: Partial view of glottis; 2b: Only posterior extremity of glottis seen or only arytenoid cartilages; 3: Only epiglottis seen, none of glottis seen; 4: Neither glottis nor epiglottis seen) | Immediately after successful endotrachel intubation | |
Secondary | V1 time | The time passed from the cutaneous incision until the measurement of V1 (pre-dissection stimulation of vagus nerve) | Immediately after vagus identification | |
Secondary | incidence of post-operative complication | The incidence of post-operative complication (paralysis of RLN, hyporparathyroidism, bleeding or infections of surgical site, dysphagia, post-operative lung complications). | At 48 hours from surgery | |
Secondary | Post-dissection vagus stimulation value | Record of the vagus stimulation (V2) with the intraoperative neuromuscular monitoring after the dissection of the thyroid | Immediately after the complete removal of the thyroid | |
Secondary | Post-dissection recurrent nerve stimulation value | Record of the recurrent nerve stimulation (R2) with the intraoperative neuromuscular monitoring at the end of the dissection of the thyroid | Immediately after the complete removal of the thyroid | |
Secondary | Pain assessment | Evaluation of postoperative pain by means of the numeric pain rating scale from 0 (no pain) to 10 (maximal severe pain) | Immediately after the end of the surgery | |
Secondary | Predissection recurrent nerve stimulation value | Record of the recurrent nerve stimulation (R1) with the intraoperative neuromuscular monitoring before the dissection of the thyroid | Immediately after recurrent nerve identification | |
Secondary | Predissection vagus stimulation value | Record of the vagus stimulation (V1) with the intraoperative neuromuscular monitoring before the dissection of the thyroid | Immediately after vagus identification |
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