Use of Perfusion Index Change as a Predictor of Hypotension During Propofol Sedation in Adult Patients Undergoing Hip Surgery Under Spinal Anesthesia: A Prospective Observational Study

Samsung Medical Center

Status: Completed

Conditions: Hypotension; Spinal Anesthetics Causing Adverse Effects in Therapeutic Use

Treatments: Other: Observation

Study type: Observational

Funder types: Other

Identifiers

NCT03556969

2018-03-052

Details and patient eligibility

About

This observational study is to evaluate Perfusion Index Change as a Predictor of Hypotension During Propofol Sedation in Adult Patients Undergoing Hip Surgery Under Spinal Anesthesia.

Enrollment: 39 patients

Sex: All

Ages: 19+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Adult patients having hip surgery under spinal anesthesia and propofol sedation

Exclusion criteria

• ASA class IV or above
• pregnancy
• inability to measure noninvasive blood pressure on the arm
• preexisting hemodynamic instability
• known peripheral artery occlusive disease
• known autonomic nerve dysfunction
• uncontrolled hypertension

Trial design

39 participants in 1 patient group

Propofol sedation after SA

Description:

Participants who undergo propofol sedation after spinal anesthesia

Treatment:

Other: Observation