Erector Spinae Plane Block Reduces Postoperative Pain Following Laparoscopic Colorectal Operation

NCT04238780 — Not applicable, Unknown, 60 participants, Gachon University Gil Medical Center

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

RegistryNCT04238780
StatusUnknown
PhaseNot applicable
Study typeInterventional; randomized, parallel, masking: quadruple, treatment
Enrollment60 (Estimated)
SponsorGachon University Gil Medical Center (Other)
ConditionsPostoperative Pain
InterventionsErector Spinae Plane Block, Intravenous fentanyl patient control device (Procedure)
Datesstart 2020-02-20, primary completion 2023-06-20, completion 2023-12-20 (estimated), first posted 2020-01-23, last updated 2023-09-13
Locations1 site in South Korea

Related Papers Related Patents Related Grants Related Experts
All trials for Postoperative Pain All trials of Erector Spinae Plane Block All trials of Intravenous fentanyl patient control device

-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.

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+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.

+Arms and interventions

ArmTypeInterventionsDescription
ESP( Erector Spinae Plane Block)Active comparatorProcedure: Erector Spinae Plane Block; Procedure: Intravenous fentanyl patient control deviceAfter 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.
control groupActive comparatorProcedure: Intravenous fentanyl patient control deviceNo regional anesthesia technique will be applied to the control group. Intravenous fentanyl patient control device 24-hour fentanyl consumption will be recorded.
  • Erector Spinae Plane Block (Procedure): 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 (Procedure): 24-hour fentanyl consumption will be recorded.

+Outcome measures

Primary outcomes

  • numerical rating scale on rest and cough [24 hours after surgery]: In the recovery room, post op 6hours, post op 24 hours

Secondary outcomes

  • opioid consumption [24 hours after surgery]: In the recovery room, post op 6hours, post op 24 hours
  • 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

+Eligibility

Sex: All, ages: 20 Years to 70 Years

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)

+Locations (1)

FacilityCityCountryStatus
Gachon University College of Medicine, Gil HospitalIncheonSouth KoreaRecruiting

+Investigators

  • hyunjeong kwack, md,phd, Study director, Gachon University Gil Medical Center