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Ultrasound-Guided Erector Spinae Plan Block in Patients Undergoing ESWL

A

Ataturk University

Status

Unknown

Conditions

Urinary System Stones
Pain

Treatments

Drug: Bupivacaine HCl 0.5 % in 10 ml and 2 % lidocaine in 10 ml
Drug: 5 % Lidocaine Topical Gel and 800 mg ibuprofen intravenously

Study type

Interventional

Funder types

Other

Identifiers

NCT04213924
ESPB for ESWL

Details and patient eligibility

About

Extracorporeal shock wave lithotripsy (ESWL) is widely used in the treatment of urinary tract stones and is generally applied to outpatients. To achieve fragmentation in ESWL, shock waves must be applied with sufficient power and time. Providing effective analgesia during this procedure is crucial to the success of the procedure. Erector Spinae Plan Block (ESPB) was first described in 2016 and, it is frequently used for postoperative analgesia in urinary system surgery. This study aimed to investigate the efficacy of ESPB in patients undergoing ESWL.

Enrollment

60 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • American Society of Anesthesiologist's physiologic state I-II patients undergoing Extracorporeal Shockwave Lithotripsy

Exclusion criteria

  • chronic pain
  • bleeding disorders
  • renal or hepatic insufficiency
  • patients on chronic non-steroidal anti-inflammatory medications
  • emergency cases

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

60 participants in 2 patient groups

Group ESPB
Active Comparator group
Description:
Ultrasound-guided erector spinae plane block with 10 ml %0.5 bupivacaine and 10 ml %2 lidocaine
Treatment:
Drug: Bupivacaine HCl 0.5 % in 10 ml and 2 % lidocaine in 10 ml
Group NSAII
Active Comparator group
Description:
lidocaine 5% gel and 800 mg ibuprofen intravenously
Treatment:
Drug: 5 % Lidocaine Topical Gel and 800 mg ibuprofen intravenously

Trial contacts and locations

1

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Central trial contact

Ahmet Yayik, MD; Ali Ahiskalioglu, MD

Data sourced from clinicaltrials.gov

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