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UnknownNCT04656821

Erector Spinae Block Versus Thoracic Paravertebral Block for Acute Thoracic Herpes Zoster

Ultrasound Guided Erector Spinae Block Versus Ultrasound Guided Thoracic Paravertebral Block for Pain Relief in Patients With Acute Thoracic Herpes Zoster

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
90 (estimated)
Sponsor
Tanta University · Academic / Other
Sex
All
Age
51 Years – 75 Years
Healthy volunteers
Not accepted

Summary

The aim of this research is to study and compare the efficacy and safety of single injection erector spinae plane block and thoracic paravertebral block in prevention of post herpetic neuralgia in patients with acute thoracic herpes zoster.

Conditions

Interventions

TypeNameDescription
DRUGControl RxPatients of this group will receive standard treatment for herpes zoster which include acyclovir 800 mg, 5 times daily administered orally within the first 72 hours and analgesics as needed
PROCEDUREErector Spinae BlockPatients of this group will receive 25 mg bupivacaine 0.5%, plus 8 mg dexamethasone in a total volume of 10 ml (The final concentration of bupivacaine will be 0.25%) to be injected beneath the erector spinae muscle sheath) at the desired level under ultrasonography.
PROCEDUREThoracic Paravertebral BlockPatients of this group will receive 25 mg bupivacaine 0.5% , plus 8mg dexamethasone in a total volume of 10 ml(The final concentration of bupivacaine will be 0.25%) to be injected in the Paravertebral space at desired level under ultrasonography

Timeline

Start date
2020-12-05
Primary completion
2021-06-06
Completion
2021-06-20
First posted
2020-12-07
Last updated
2020-12-08

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT04656821. Inclusion in this directory is not an endorsement.