Effect of Ultrasound-guided Erector Spinae Plane Block on postoperative recovery of patients undergoing laparoscopic colon cancer surgery

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2300073180

Enrollment

Unknown

Registered

2023-07-04

Start date

2023-07-01

Completion date

Unknown

Last updated

2023-07-10

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

Conditions

Colon cancer

Interventions

E group:Ultrasound-guided Erector Spinae Plane Block

C group:No intervention

Eligibility

Sex/Gender

All

Age

35 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1: Age 35-65 years 2: BMI18.5-28kg/m2 3: ASA I-III 4: Undergoing laparoscopic colon cancer surgery in the operating room of Beijing Friendship Hospital 5: Patients who voluntarily use an analgesia pump

Exclusion criteria

Exclusion criteria: 1: Inability or refusal to sign on the research informed consent form 2: Patients who are unable to fit in a lateral position 3: Infection at the Erector Spinae Plane block area 4: Pregnancy 5: History of long-term chronic pain before surgery 6: Regularly taken antalgic within 3 months before surgery 7: Allergic to ropivacaine or has liver and kidney diseases that may affect the metabolism of drug 8: Has the same underlying disease as local anesthetic intoxication, such as epilepsy

Design outcomes

Primary

Measure	Time frame
Score of QoR-15;Perioperative satisfaction;	—

Secondary

Measure	Time frame
Total intraoperative opioids;Intraoperative propofol dosage;First exhaust time;Times of the analgesic pump been pressed;	—

Countries

China

Contacts

Public ContactFushan Xue

Beijing Friendship Hospital affiliated to Capital Medical University

xuefushan@aliyun.com+86 139 1117 7655

Outcome results

None listed

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