Skip to content

Evaluation of surgical condition during Interventional Neuroradiology (INR) in patients with deep vs moderate neuromuscular block

Evaluation of surgical condition during Interventional Neuroradiology (INR) in patients with deep vs moderate neuromuscular block - Evaluation of surgical condition during Interventional Neuroradiology (INR) in patients with deep vs moderate neuromuscular block

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000033178
Enrollment
58
Registered
2018-07-06
Start date
2018-07-02
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Randomized controlled observational study

Interventions

In the course of performing interventional procedures of cerebrovascular disease under general anesthesia, one of two methods of using muscle relaxant is selected randomly. 1. deep neuromuscular bl
s ulnar nerve, and maintained a deep muscle relaxation state, PTC count 1-2, in the experimental group. A. TOF count of 3 or more: Rocuronium 0.15 mg / kg is administered in both experimental and c

Sponsors

Seoul National University Bundang Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: The American Society of Anesthesiologists (ASA) Class I and II patients who were admitted to our institution to undergo regular surgery were enrolled in this study.

Exclusion criteria

Exclusion criteria: 1. American Academy of Anesthesiology ASA physical classification 3 or 4 2. Patients with a history of myasthenia gravis 3. Patients with renal impairment: serum creatinine more than 2 times normal, urine volume <0.5 ml / kg / hr, GFR <60 ml / hr, with proteinuria 4. Patients with allergy to rocuronium 5. Patients with a history of malignant hypertension 6. 18.5 kg / m2 <BMI <30 kg / m2 does not fall into this category 7. Patients who refuse to participate in the study or can not receive informed consent

Design outcomes

Primary

MeasureTime frame
surgical condition rating by surgeon

Secondary

MeasureTime frame
recovery time, hemodynamic change

Countries

Asia(except Japan)

Contacts

Public ContactBo Young Kim

Seoul National University Bundang Hospital Department of Anesthesiology and Pain Medicine

notinvasive@gmail.com82-31-787-7499

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026