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Erector Spinae Plane Block with Dexmedetomidine and Bupivacain Versus Dexamethasone and Bupivacain for Postoperative Analgesia in Patients Undergoing Abdominal Surgeries

L

Loay Gamal

Status and phase

Not yet enrolling
Phase 1

Conditions

Analgesia, Postoperative

Treatments

Procedure: Erector Spinae Plane Block

Study type

Interventional

Funder types

Other

Identifiers

NCT06658418
erector spinae plane block

Details and patient eligibility

About

To compare the analgesic effect of dexmedetomidine combined with bupivacaine versus dexamethasone combined with bupivacaine for ultrasound-guided ESPB for postoperative pain control in patients scheduled for abdominal surgeries

Enrollment

90 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Age :18 years old and older. Patients undergoing open abdominal surgery.

Exclusion criteria

  1. Patient refusal
  2. known sensitivity or contraindication to any of study drugs
  3. contraindications for local anesthesia
  4. Patients with local infection at site of puncture
  5. uncooperative patients
  6. history of psychological disorders or chronic pain and significant liver or renal disease.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

90 participants in 2 patient groups

dexmedetomidine combined with bupivacaine
Active Comparator group
Description:
use for Dexmedetomidine and bupivacain for erector spinae plane block
Treatment:
Procedure: Erector Spinae Plane Block
dexamethasone combined with bupivacaine
Experimental group
Description:
use of dexamethasone combined with bupivacaine for erector spinae plane block
Treatment:
Procedure: Erector Spinae Plane Block

Trial contacts and locations

0

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Central trial contact

loay GAMAL loay Gamal, master

Data sourced from clinicaltrials.gov

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