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Diaphragm Ultrasound to Predict Posteroperative Residual Blockade

Diaphragm Ultrasound to Predict Posteroperative Residual Blockade

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04321681
Enrollment
75
Registered
2020-03-25
Start date
2019-06-01
Completion date
2020-04-30
Last updated
2020-03-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Residual Curarization, Ultrasonography

Brief summary

This study is a prospective observational research approved by the Ethics Committee of the Peking Union medical college Hospital. Patients scheduled for elective non-abdominal and non-thoracic surgery among age of 19-65 years and American Society of Anesthesiologists Physical Status Classification(ASA) I or II were inrolled. Diaphragm ultrasonogram was measured pre and post operation. Diaphragm excursion and diaphragm thickening fraction during quiet breathing as well as deep breathing were assessed. Neuromuscular monitor was performed during operation, after proper calibration.

Interventions

OTHERno intervention

no intervention

Sponsors

Peking Union Medical College Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

Enrollment criteria: 1. Patients who were scheduled for elective non-abdominal and non-thoracic surgery in Peking Union medical college hospital. 2. age of 19-65 years 3. American Society of Anesthesiologists Physical Status Classification(ASA) I or II. 4. Agree to informed consent

Exclusion criteria

: Patients with neuromuscular diseases, diaphragmatic palsy, thoracic malformation, hand disabilities, chronic obstructive pulmonary disease, severe liver or kidney diseases, electrolyte or acid-base disorders, morbid obesity (body mass index ≥30 kg/m2), pregnancy, allergy to drugs used in the study, use of medication interfering neuromuscular transmission within 72hours and patients with predicted difficulty in maintenance of airway were excluded from this study. Written informed consent will be obtained before preoperative evaluation by an anesthesiologist.

Design outcomes

Primary

MeasureTime frameDescription
TOFr at extubationwithin1 min before extubationNeuromuscular function was monitored thoughout operation based neuromuscular monitoring guideline by an independent investigator. TOF ratio before extubation was recorded. The scale of TOFr range from 0 to 1. TOFr\<0.9 indicate existance of residual neuromuscular blockade.
Diaphragm ultrasound parameterwithin 1 min after extubationDiaphragm excursion and thickening fraction was measured through ultrasonography within 2 min after extubation. Correlation between TOFr ratio and diaphragm parameters was explored.

Secondary

MeasureTime frameDescription
reintubation ratewithin 24 hourIf patients cannot breath by themselves after extubation, They need to be reintubated and mechanical ventilation need to be use to sustain their breathing.
Posteroperative pulmonary complication1 monthincidence of airway obstruction, bronchospasm, pulmonary aspiration of gastric contents, apnea, unexpected ICU admissions, atelectasis and pneumonia

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026