Trials / Unknown
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
| Type | Name | Description |
|---|---|---|
| DRUG | Control Rx | Patients 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 |
| PROCEDURE | Erector Spinae Block | Patients 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. |
| PROCEDURE | Thoracic Paravertebral Block | Patients 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.