influence of different sensory blockade after erector spinae plane block on postoperative pain and quality of recovery in patients undergoing video-assisted thoracic surgery

anesthesia and analgesia

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2200062974

Enrollment

Unknown

Registered

2022-08-25

Start date

2022-08-24

Completion date

Unknown

Last updated

2023-04-12

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

Conditions

postoperative pain

Interventions

group hypoaesthesia:single-injection of ESPB

normal sensation group:single-injection of ESPB

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. Both male and female, aged 18-65 2.BMI 18-30kg/m2, ASA 1-2 3. Voluntarily accept the postoperative analgesic pump 4.Patients who underwent thoracoscopic partial lung surgery / pulmonary wedge surgery / lung artillery surgery; 5. the informed consent was obtained from all patients

Exclusion criteria

Exclusion criteria: 1. Allergic to local anesthetics or non-steroidal anti-inflammatory drugs 2. Known coagulopathy 3. Infection near the puncture 4. History of chronic pain or regular analgesic usage 5. Patients with communication disorders or other reasons not applicable to this study were excluded

Design outcomes

Primary

Measure	Time frame
postoperative quality of recovery-15;	—

Secondary

Measure	Time frame
Time of first rescue analgesia;24 h cumultive sufentanil consumption;analgesia satisfaction score;postoperative NRS score;	—

Countries

China

Contacts

Public Contactlili zhang

799193482@qq.com13955129453

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026