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Dexamethasone and Block Duration in Upper Extremity

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The University of Chicago

Status

Terminated

Conditions

Duration of Pain Relief

Treatments

Drug: Dexamthsone
Drug: Bupivacaine

Study type

Interventional

Funder types

Other

Identifiers

NCT01756573
IRB12-2192

Details and patient eligibility

About

Effect of dexamethasone on prolonging upper extremity block is well known. But it not known if the effect comes from its local effect on the nerves or from its general analgesic effect. In this study we will compare the systemic effect to its local effect to find out if there is a difference or not.

Enrollment

5 patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • age 18-75, no contraindication to regional anesthesia,

Exclusion criteria

  • opioid user, chronic pain conditions, peripheral neuropathy

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

5 participants in 3 patient groups

Bupivacaine
Active Comparator group
Description:
Control
Treatment:
Drug: Bupivacaine
Bupivacaine with Dexamethasone
Experimental group
Description:
Dexamethasone will be mixed with bupivacaine
Treatment:
Drug: Dexamthsone
Drug: Bupivacaine
Intravenous Dexamethasone
Active Comparator group
Description:
Dexamethasone will be given intravenously
Treatment:
Drug: Dexamthsone
Drug: Bupivacaine

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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