Effect of neuromuscular blockers in patients undergoing the day surgery

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0004285

Enrollment

Registered

2019-09-06

Start date

2018-11-13

Completion date

Unknown

Last updated

2021-01-06

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

Conditions

None listed

Interventions

Drug : At induction, participant are divided into 3 groups according to the drugs administered by IV Control group : Fresofol 2mg/kg + saline 3cc Fentanyl group : Fresofol 2mg/kg + (Fentanyl 1mcg/kg +

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: 1. Female patients under 20 years old and under 65 years of age who undergo general anesthesia 2. American Society of Anesthesiologists classification (ASA class) 1,2 grade 3. Patients with a body mass index (BMI) range of 18-30 kg / m2

Exclusion criteria

Exclusion criteria: 1. Patients who do not agree with the clinical trial 2. American Society of Anesthesiologists classification 3 or 4 3. The pregnant patient 4. Patients with history of Allergy in Rocuronium

Design outcomes

Primary

Measure	Time frame
blood pressure, pulse, bispectral index, movement score (cough, chin, limb), postoperative motion, self-respiration, extubation time	—

Secondary

Measure	Time frame
dizziness in recovery room, first urine time after operation, Postoperative gross movement, Surgeon's satisfaction, Unexpected Hospitalization	—

Countries

Korea, Republic of

Contacts

Public ContactKuen Su Lee

Korea University Ansan Hospital

Outcome results