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Midazolam Versus Dexamethasone as an Adjuvant to Local Anesthetics in the Ultrasound Guided Hydrodissection of Median Nerve for Treatment of Carpal Tunnel Syndrome Patients

Midazolam Versus Dexamethasone as an Adjuvant to Local Anesthetics in the Ultrasound Guided Hydrodissection of Median Nerve for Treatment of Carpal Tunnel Syndrome Patients

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04527770
Enrollment
134
Registered
2020-08-27
Start date
2020-09-01
Completion date
2021-04-30
Last updated
2022-02-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pain Syndrome

Keywords

Midazolam, median nerve, dexamethasone

Brief summary

midazolam and dexamethasone both can counteract chronic pain. either via GABA mimetic action or via anti prostaglandins

Detailed description

Entrapement syndrome - namely median nerve compression in carpal tunnel syndrome - causes chronic pain that can be refractory to medical treatment . Ultrasound guided hydrodissection is an option for alleviating pain . Recurrence is the main side effect of injection. We try in this research to prevent recurrence rate . Midazolam and dexamethasone both are used in chronic pain . Midazolm act by GABA mimetic action while dexamethasone act by decrease interleukin formation

Interventions

DRUGDexamethasone

Ultrasound guided median nerve hydrodiseection using dexamethasone or midazolam

DRUGMidazolam injection

intracarpal injection of midazolam and bupivacaine 0.5%

Sponsors

Minia University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Masking description

both drugs are the same colour and volume injected by a staff member not aware of study design

Intervention model description

2 groups received hydrodissection sonar guided , one group received 50 mic/kg midazolam and the other received 8 mg dexamethasone

Eligibility

Sex/Gender
ALL
Age
30 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* numbness or pain in the nerve distribution, nerve conduction studies (NCS) corresponding with AANEM guidelines * Nerve cross sectional area \>12mm2

Exclusion criteria

* Refusal to participate * History of operation in median nerve.were patient refusal to participate, pain recurrence after previous injection and severe symptoms requiring surgical release, diabetic patients

Design outcomes

Primary

MeasureTime frameDescription
comparing efficacy of midazolam against dexmethasone in combination with bupivacaine 0.5%up to 6 monthsuse of visual analogue score

Secondary

MeasureTime frameDescription
Subjective pain assesmentup to 6 monthsBOSTON questionnaire
complicationspain recurrence after 6 months, neurotoxicity immediately after injectionneurotoxicity, pain recurrence after injection
Nerve electrophysiologyup to 6 monthssensory nerve conduction , distal motor latency.
nerve sonogramup to 6 monthsnerve cross sectional area.

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026