Erector Spinae Plane Block Reduces Postoperative Pain Following Laparoscopic Colorectal Operation

Not Applicable

Recruiting

• Conditions: Postoperative Pain
• Interventions: Procedure: Intravenous fentanyl patient control device; Procedure: Erector Spinae Plane Block

• Registration Number: NCT04238780
• Lead Sponsor: Gachon University Gil Medical Center

Brief Summary

The goal of this study is to evaluate the effect of ultrasound guided erector spinae plane block on postoperative pain and quality of recovery after laparoscopic colon surgery.

Detailed Description

.The goal of this study is to evaluate the effect of ultrasound guided erector spinae plane block on postoperative pain and quality of recovery after laparoscopic colon surgery.

Study Timeline

• Study First Submitted: 2020-01-20
• Study First Submitted QC: 2020-01-20
• Study First Posted: 2020-01-23
• Study Start: 2020-02-20
• Primary Completion: 2023-06-20
• Status Verified: 2023-09
• Last Update Submitted: 2023-09-11
• Last Update Posted: 2023-09-13
• Study Completion: 2023-12-20

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

• aged between 20 and 70 years, with an American Society of Anesthesiologists physical status of 1 or 2, who were scheduled for laparoscopic colorectal operation

Exclusion Criteria

• sensitivity to local anesthetic, bleeding disorders , receiving anticoagulant, body mass index (BMI) over 35/kg/m2 spine or chest wall deformity pregnancy tolerance to opioid analgesics inability to use patient-controlled analgesia (PCA)

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
control group	Intravenous fentanyl patient control device	No regional anesthesia technique will be applied to the control group. Intravenous fentanyl patient control device 24-hour fentanyl consumption will be recorded.
ESP( Erector Spinae Plane Block)	Erector Spinae Plane Block	After induction parturient in the ESPB underwent bilateral ESPB at the level of T7 using a linear ultrasound (US) transducer. Intravenous fentanyl patient control device 24-hour fentanyl consumption will be recorded.
ESP( Erector Spinae Plane Block)	Intravenous fentanyl patient control device	After induction parturient in the ESPB underwent bilateral ESPB at the level of T7 using a linear ultrasound (US) transducer. Intravenous fentanyl patient control device 24-hour fentanyl consumption will be recorded.

Primary Outcome Measures

Name	Time	Method
numerical rating scale on rest and cough	24 hours after surgery	In the recovery room, post op 6hours, post op 24 hours

Secondary Outcome Measures

Name	Time	Method
Quality of Recovery	1day before operation, post op 24 hours	pre operative QoR 40 scores compares
need for analgesics	24 hours after surgery	Number of patients who required analgesic in the first 24 hour
opioid consumption	24 hours after surgery	In the recovery room, post op 6hours, post op 24 hours

Trial Locations

Locations (1)

Gachon University College of Medicine, Gil Hospital; 🇰🇷 Incheon, Korea, Republic of