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U/s Guided Oblique Subcostal Transversus Abdominis Plane Block Versus Erector Spinae Plane Block as Preemptive Analgesia

B

Benha University

Status and phase

Completed
Phase 4

Conditions

Hernia, Umbilical
Pain

Treatments

Drug: Bupivacain
Drug: Bupivacaine

Study type

Interventional

Funder types

Other

Identifiers

NCT04941170
RC 2-6-2021

Details and patient eligibility

About

Administration of opioids for the treatment of acute pain after open umbilical hernia repair is associated with many side effects. Erector spinae plane (ESP) block is a novel inter-fascial plane block used in postoperative pain and chronic neuropathic pain relief of the thoracoabdominal region.TAP block is a regional injection of local anaesthetic between the transversus abdominis and internal oblique muscle planes. TAP block affects the sensory nerves of the anterolateral abdominal wall (T6-L1) that innervate the abdomen.

Full description

TAP block is a regional injection of local anaesthetic between the transversus abdominis and internal oblique muscle planes. TAP block affects the sensory nerves of the anterolateral abdominal wall (T6-L1) that innervate the abdomen. TAP block is an easy technique and decreases postoperative pain and opioid consumption.

Erector spinae plane (ESP) block is a novel inter-fascial plane block used in postoperative pain and chronic neuropathic pain relief of the thoracoabdominal region. However, its first use was for the treatment of chronic pain, but recently it has been used as a postoperative regional analgesia technique in different surgeries from the shoulder to hip regions (3-4) The present study will be carried out to compare the preemptive analgesic efficacy between the ultrasound-guided bilateral ESP block versus bilateral oblique subcostal TAP block on patients undergoing open umbilical hernia repair.

Enrollment

70 patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. American Society of anesthesiologists I-II, scheduled for open umbilical hernia repair.
  2. Age range of 18-65 years.

Exclusion criteria

  1. patient refusal.
  2. Patients belonging to ASA grade III and grade IV.
  3. Extreme obesity (BMI >35).
  4. hepatic or renal insufficiency.
  5. preoperative cognitive dysfunction or communication disorder.
  6. allergy to amide-type local anaesthetics.
  7. back puncture site infection.
  8. Coagulation disorders, pregnancy, drug abusers.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

70 participants in 2 patient groups

Group (T)
Active Comparator group
Description:
receive preoperative bilateral ultrasound-guided oblique subcostal transversus abdominis plane block.
Treatment:
Drug: Bupivacaine
Drug: Bupivacain
Group (E)
Active Comparator group
Description:
receive preoperative bilateral ultrasound-guided erector spinae plane block.
Treatment:
Drug: Bupivacaine
Drug: Bupivacain

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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