Skip to content

Effect of Ultrasound-Guided External Oblique Intercostal Plane Block on the Postoperative Analgesia and the Quality of Recovery in Patients Undergoing upper abdominal surgery

Effect of Ultrasound-Guided External Oblique Intercostal Plane Block on the Postoperative Analgesia and the Quality of Recovery in Patients Undergoing upper abdominal surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400080461
Enrollment
Unknown
Registered
2024-01-30
Start date
2024-02-02
Completion date
Unknown
Last updated
2024-02-05

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

Conditions

Patients undergoing upper abdominal surgery

Interventions

External oblique intercostal plane block group :After induction of general anesthesia, ultrasound guided bilateral external oblique intercostal plane block was performed

Sponsors

The First Affiliated Hospital of Anhui Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Patients aged 18 to 65 years 2.ASA grade? to ? 3.Patients with upper abdominal surgery such as laparoscopic gallbladder, liver and stomach surgery 4.Patients who are not expected to be admitted to ICU after surgery 5.Patients who agreed to participate in the study and signed informed consent

Exclusion criteria

Exclusion criteria: 1.Severe abnormal coagulation function 2.Infection of the puncture site 3.Allergies to local anesthetics 4.History of chronic pain or neuropathic pain 5.Mental illness,such as schizophrenia, depression, epilepsy, history of chronic analgesic drug use, history of alcoholism, opioid dependence 6.Unable to cooperate with the researcher for any reason, such as hearing or vision impairment, language comprehension impairment, and inability to understand the QOR-15 scale content 7.Parkinson's Disease, Alzheimer's disease, insomnia, severe liver insufficiency (ChildC) Renal insufficiency (preoperative dialysis) 8.Preoperative life can not take care of themselves 9.Intravenous analgesia pumps were not available after surgery

Design outcomes

Primary

MeasureTime frame
QoR-15 score 24 hours after surgery;

Secondary

MeasureTime frame
Analgesic pump opioid consumption 48 hours after surgery;NRS pain scores at rest and exercise at different time points after surgery;Number of postoperative relief analgesia;

Countries

China

Contacts

Public ContactZuo Youmei

The First Affiliated Hospital of Anhui Medical University

zuoyoumei_2012@163.com+86 181 5653 7618

Outcome results

None listed

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