Erector Spinae Block Versus PECS Block Type II for Breast Surgeries

NACompletedINTERVENTIONAL
Enrollment

60

Participants

Timeline

Start Date

March 19, 2020

Primary Completion Date

March 10, 2021

Study Completion Date

March 10, 2021

Conditions
Analgesia
Interventions
OTHER

Erector Spinae block

Patient in the prone position 20 min before induction of general anesthesia. Skin is sterilized by 10% povidone iodine. An US multifrequency convex probe (1-8 MHz) will be used for block. A 22G, 50-mm in length needle will be used and block will be performed at the T4 level of the spine using in-plane approach where a convex probe is placed 2-3 cm lateral to the spine using sagittal approach. Erector spinae muscle and the transverse processes are located and the needle will be inserted deep into the muscle. The needle is directed craniotomy-caudally. Correct position of the needle tip is confirmed with administration of 0.5-1 ml of local anesthetic to monitor spread then 20 ml of 0.25% bupivacaine will be administered for block performance. Distribution of local anesthetic is monitored in both cranial and caudal directions

Trial Locations (1)

02002

NCI Egypt, Cairo

All Listed Sponsors
lead

National Cancer Institute, Egypt

OTHER

NCT04284124 - Erector Spinae Block Versus PECS Block Type II for Breast Surgeries | Biotech Hunter | Biotech Hunter