Efficacy of ultrasound guided erector spinae block for postoperative analgesia after breast conserving surgery

Efficacy of ultrasound guided erector spinae block for postoperative analgesia after breast conserving surgery: a randomized controlled trial

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0002744

Enrollment

Registered

2018-03-21

Start date

2018-03-10

Completion date

Unknown

Last updated

2022-05-02

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 : The control group, which did not perform the block, and the experimental group, which performed the erector spinae plane block were set. Drug was injected into the deep fascia of t

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: Patients who planed a breast surgery with a breast cancer between the ages of 20 and 65

Exclusion criteria

Exclusion criteria: Patients with chronic pain, those who are recently receiving opioids, corticosteroids and other pain medications, patients with cardiopulmonary dysfunction, impaired liver function and renal function, patients with evidence of infection, patients with bleeding tendency, pregnant women, allergic patients, Intravenous Patient Controlled Analgesia for postoperative pain control, patients and caregivers do not agree with the study

Design outcomes

Primary

Measure	Time frame
Pain score	—

Secondary

Measure	Time frame
Additional analgesic dose after surgery	—

Countries

Korea, Republic of

Contacts

Public ContactWon-joong Kim

Ewha Womans University Medical Center

ickypoo@naver.com+82-2-2650-2829

Outcome results