The application of ultrasound-guided erector spinae plane block and oblique subcostal transversus abdominis plane block in postoperative pain management after laparoscopic cholecystectomy

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2400081972

Enrollment

Unknown

Registered

2024-03-18

Start date

2024-03-18

Completion date

Unknown

Last updated

2024-03-25

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

Conditions

chronic cholecystitis

Interventions

Control group:Incision block

ESPB group:Ultrasound-guided erector spinal plane block

OSTAPB group:Ultrasound guided oblique subcostal transversal plane block

Eligibility

Sex/Gender

All

Age

18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1) 18 years old = age =70 years old, regardless of gender or ethnicity; 2) Laparoscopic cholecystectomy under elective general anesthesia; 3) ASA?~? grade; 4) Suitable for regional anesthesia; 5) Agree to participate in the study and sign the informed consent;

Exclusion criteria

Exclusion criteria: 1) Allergic to the investigational drug or to local anesthetic drugs; 2) A history of opioid abuse; 3) There is skin infection at the site of blocked puncture; 4) Suffering from peripheral neuropathy; 5) Abnormal coagulation function, i.e. prothrombin time or activated partial prothrombin time exceeds the standard value, or the International Normalized ratio (INR) is greater than 1.4, or the platelet count is less than 80 x 10^9/l; 6) Severe renal function impairment (kidney replacement therapy required); 7) Severe liver function impairment (Child-Pugh grade C); 8) Patients and their families request analgesic pumps; 9) The attending physician or researcher considers that there are other circumstances that are not suitable for participation in this study;

Design outcomes

Primary

Measure	Time frame
VAS;	—

Secondary

Measure	Time frame
Intraoperative doses of opioids were administered;Salvage analgesics were used within 24 hours after surgery;Postoperative NRS pain score;Sleep disruption due to pain;First walking time;Incidence of postoperative adverse reactions such as nausea, vomiting, dizziness and urinary retention;Incidence of local anesthesia poisoning;The incidence of nerve block complications such as infection, bleeding and nerve injury at puncture site;	—

Measure

Time frame

Intraoperative doses of opioids were administered;Salvage analgesics were used within 24 hours after surgery;Postoperative NRS pain score;Sleep disruption due to pain;First walking time;Incidence of postoperative adverse reactions such as nausea, vomiting, dizziness and urinary retention;Incidence of local anesthesia poisoning;The incidence of nerve block complications such as infection, bleeding and nerve injury at puncture site;

—

Countries

CHINA

Contacts

Public ContactYEZHENHAI

Department of Anesthesiology, People's Hospital of Ningxia Hui Autonomous Region

13619506202@163.com+86 136 1950 6202

Outcome results

None listed

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