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Erector Spinae Plane Block Versus Oblique Subcostal Transverses Abdominis Plane Block

Z

Zagazig University

Status

Enrolling

Conditions

Postoperative Pain

Treatments

Procedure: oblique subcostal transverse abdominis plane (TAP) block
Procedure: erector spinae plane (ESP) block

Study type

Interventional

Funder types

Other

Identifiers

NCT05286125
8034-7-11-2021

Details and patient eligibility

About

Comparing the impact of bilateral erector spinae plane block and transverse abdominis plane block on improving quality of pain management after umbilical hernia repair.

Full description

Postoperative pain is an important problem after umbilical hernia repair which has negative effects on patient's hemodynamics and cause delayed ambulation resulting in prolonged duration of hospital stay and poor patient satisfaction.

Multiple analgesic strategies have been proposed including Non steroidal anti-inflammatory drugs (NSAIDs), opioids, epidural analgesia. Each of them has its limitations.

Ultra¬sound guided regional anesthesia techniques for abdominal wall can be effective components of multimodal postoperative analgesia with limited side-effects Erector spinae plane (ESP) block is a promising para-spinal bock that can achieve both visceral and somatic abdominal analgesia if the injection was performed at a lower thoracic level. Transverse abdominis plane (TAP) block which is considered a peripheral nerve block that is aimed at anesthetizing nerves supplying the anterior abdominal wall.

We will compare between erector spinae plane block and transverse abdominis plane block for controlling postoperative pain after umbilical hernia repair.

Patients will be allocated randomly into two equal groups by a computer-generated randomization table Group (E) (n=26): Patients will receive erector spinae plane (ESP) block after completion of surgery.

Group (T) (n= 26): Patients will receive oblique subcostal transverse abdominis plane (TAP) block after completion of surgery

Enrollment

52 estimated patients

Sex

All

Ages

21 to 60 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patients scheduled for elective umbilical hernia repair.
  • Patient acceptance.
  • Both sex
  • Patient's age 21 - 60 years.
  • Patients with American Society of Anesthesiologists (ASA) physical status I, II.
  • BMI 25 - 30 kg m-2.

Exclusion criteria

  • Uncooperative patients and patients with psychological problems.
  • Patients with liver or renal impairment.
  • Patients with contraindication to regional anesthesia.
  • Patients with history of allergy to drug used in the study.
  • Patients with chronic pain.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

52 participants in 2 patient groups

erector spinae plane (ESP) block group ( (E) group)
Active Comparator group
Description:
Under aseptic conditions, a high frequency linear transducer will be placed on the spinous process at T8 level on the parasagittal plane and then slid 2.5-3 cm laterally to visualize the transverse process and erector spinae muscle.
Treatment:
Procedure: erector spinae plane (ESP) block
oblique subcostal transverse abdominis plane (TAP) block ( (T) group) )
Active Comparator group
Description:
Under aseptic conditions, the probe will be initially placed below the xyphoid process to view the linea alba, then directed obliquely down the costal margin while keeping the rectus abdominis muscle in view. The transverse abdominis muscle come into view below the rectus abdominis muscle. The probe will be advanced further until the semilunaris is viewed.
Treatment:
Procedure: oblique subcostal transverse abdominis plane (TAP) block

Trial contacts and locations

1

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Central trial contact

michael A shaker, lecturer; salwa s ElSherbeny, lecturer

Data sourced from clinicaltrials.gov

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