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NCT04118101

Erector Spinae Plane Block

Completed Phase 2, PHASE3 Last updated 2 April 2021
What this trial tests

Phase 2, PHASE3 trial testing ESPB block in Post Operative Pain in 46 participants. Completed in 15 February 2021.

Timeline
25 October 2019
Primary endpoint
10 December 2020
15 February 2021

Quick facts

Lead sponsorTheodor Bilharz Research Institute
PhasePhase 2, PHASE3
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposetreatment
Enrollment46
Start date25 October 2019
Primary completion10 December 2020
Estimated completion15 February 2021
Sites1 location across Egypt

Drugs / interventions tested

Conditions studied

Sponsor

Theodor Bilharz Research Institute

Who can join

Adults 18 to 60, any sex, with Post Operative Pain. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Erector spinae plane block (ESPB) is a relatively new plane block that was first described by Forero et al. in 2016, to manage persistent neuropathic pain following malunited rib fracture and persistent post-thoracotomy neuropathic pain.It's a relatively simple, ultrasound guided block in which the local anesthetic drugs are injected in the plane between the erector spinae muscle and the vertebral transverse process.This allows the injected local anesthetics to block the ventral and dorsal rami of the spinal nerves in the paravertebral area. The literature reveals successful case reports denoting the use of ESPB for pain control in cases of acute kidney transplant,percutaneous nephrolithomy, abdominal surgeries including laparoscopic and open nephrectomy, and nephrectomy in the pediatric population. The aim of this prospective randomized controlled study is to investigate the efficacy of ESPB for pain control in adult patients undergoing open renal surgery through a flank incision with respect to pain scores, postoperative analgesia consumption and patient satisfaction.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Post Operative Pain

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