Erector Spinae Plane Block Reduces Postoperative Pain Following Laparoscopic Colorectal Operation

Postoperative Pain Clinical Trial

Official title:

Ultrasound Guided Erector Spinae Plane Block Reduces Postoperative Pain Following Laparoscopic Colorectal Operation: A Randomized Controlled Study

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04238780
• Other study ID #: ESPlapaAR
• Status: Recruiting
• Phase: N/A
• Start date: February 20, 2020
• Est. completion date: December 20, 2023

Study information

• Verified date: September 2023
• Source: Gachon University Gil Medical Center
• Contact: jungju choi, nd,phd
• Phone: 8232 460 3624
• Email: jjchoi2[@]gilhospital.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

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.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 60
• Est. completion date: December 20, 2023
• Est. primary completion date: June 20, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 20 Years to 70 Years

Eligibility

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)

Related Conditions & MeSH terms

• Pain, Postoperative
• Postoperative Pain

Intervention

Procedure:
• Erector Spinae Plane Block
The transducer was placed vertically 3cm lateral to the midline to visualize the muscles of the back, transverse process and the pleura in between the two transverse processes. After local infiltration of the needle insertion site with 2-3 ml of 2% lidocaine needle was inserted in cranial-caudal direction towards the transvers process using in plane technique until the needle cross all the muscles then interfascial injection of 20ml local anesthetics is done after ensuring negative aspiration, the procedure was repeated following the same steps on the other side of the back.
• Intravenous fentanyl patient control device
24-hour fentanyl consumption will be recorded.

Locations

Country	Name	City	State
Korea, Republic of	Gachon University College of Medicine, Gil Hospital	Incheon

Sponsors (1)

Lead Sponsor	Collaborator
Gachon University Gil Medical Center

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	numerical rating scale on rest and cough	In the recovery room, post op 6hours, post op 24 hours	24 hours after surgery
Secondary	opioid consumption	In the recovery room, post op 6hours, post op 24 hours	24 hours after surgery
Secondary	Quality of Recovery	pre operative QoR 40 scores compares	1day before operation, post op 24 hours
Secondary	need for analgesics	Number of patients who required analgesic in the first 24 hour	24 hours after surgery