Effect of norepinephrine for the prevention of hypotension after spinal anesthesia in the elderly

Effect of norepinephrine continuous infusion for the prevention of hypotension after spinal anesthesia with propofol sedation in the elderly

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CRIS

Registry ID

KCT0005046

Enrollment

Registered

2020-05-21

Start date

2020-08-16

Completion date

Unknown

Last updated

2023-03-06

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

Conditions

None listed

Interventions

Drug : Group C: normal saline-0.15cc/kg/hr, intravenously continuous infusion, from the time point that the participants take the supine position after the intrathecal injection of local anesthetics t

normal saline vs norepinephrine.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: * American Society of Anesthesiologists Physical Status 1-3 * age: equal to or older than 70 years * patients scheduled to undergo a hip surgery under spinal anesthesia with propofol sedation

Exclusion criteria

Exclusion criteria: * patients who don't agree to participate in this study * patients with uncontrolled hypertension, hyperthyroidism, dementia, symptomatic coronary artery disease, or hemoglobin <10g/dL * patients with allergy to propofol, fentanyl, or bupivacaine * patients who are cont coagulopathy, severe aortic stenosis/mitral stenosis, active infection on lumbar region * patients who are judged to be inappropriate for this study by authors

Design outcomes

Primary

Measure	Time frame
number of hypotensive episodes	—

Secondary

Measure	Time frame
complications;number of hypertensive episodes;total amount of phenylephrine administered;total amount of administered fluid;number of hypotensive episodes	—

Countries

Korea, Republic of

Contacts

Public ContactHa-Jung Kim

Asan Medical Center

alexakim06@gmail.com+82-2-3010-0338

Outcome results