Comparison of recovery quality and patient satisfaction with spinal anesthesia and combined sciatic-femoral nerve block in orthopedic lower extremity surgery

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0008083

Enrollment

128

Registered

2023-01-06

Start date

2021-10-01

Completion date

Unknown

Last updated

2023-01-10

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

Conditions

None listed

Interventions

Procedure/Surgery : Group S: In the group receiving spinal anesthesia, a single injection of bupivacaine 0.5%, 10-15 mg is administered in the spinal segment (L3/4 or L4/5 or L5/S1). Use a quincke nee

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients aged 19-80 who are undergoing regular lower extremity surgery under the knee at our orthopedic surgery clinic, who want partial anesthesia (spinal anesthesia or local nerve block anesthesia) other than general anesthesia; A Patient who reads the consent form and is able to give written consent at his/her own discretion.

Exclusion criteria

Exclusion criteria: Patients who want general anesthesia; contraindications for injection (coagulopathy, allergies); patients who are expected to have difficulty in cooperation (patients with intellectual disabilities or moderate or severe dementia or severe psychiatric diseases); pregnant or lactating women; patients who are expected to undergo surgery for more than 3 hours

Design outcomes

Primary

Measure	Time frame
Quality of Recovery-15; QoR-15	—

Secondary

Measure	Time frame
Intraoperative vital sign (blood pressure, heart rate, saturation);the consumption of patients controlled analgesia device	—

Countries

Korea, Republic of

Contacts

Public ContactSeon Woo Yoo

Jeonbuk National University Hospital

sunu2424@naver.com+82-63-250-1241

Outcome results