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Erector Spinae Plane Block Reduces Postoperative Pain Following Laparoscopic Colorectal Operation

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

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04238780
Enrollment
60
Registered
2020-01-23
Start date
2020-02-20
Completion date
2023-12-20
Last updated
2023-09-13

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

Conditions

Postoperative Pain

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.

Interventions

PROCEDUREErector 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.

24-hour fentanyl consumption will be recorded.

Sponsors

Gachon University Gil Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
20 Years to 70 Years
Healthy volunteers
No

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)

Design outcomes

Primary

MeasureTime frameDescription
numerical rating scale on rest and cough24 hours after surgeryIn the recovery room, post op 6hours, post op 24 hours

Secondary

MeasureTime frameDescription
opioid consumption24 hours after surgeryIn the recovery room, post op 6hours, post op 24 hours
Quality of Recovery1day before operation, post op 24 hourspre operative QoR 40 scores compares
need for analgesics24 hours after surgeryNumber of patients who required analgesic in the first 24 hour

Countries

South Korea

Contacts

Primary Contactjungju choi, nd,phd
jjchoi2@gilhospital.com8232 460 3624

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026