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Dexamethasone and Analgesic Duration After Supraclavicular Brachial Plexus Blockade

University Health Network, Toronto logo

University Health Network, Toronto

Status

Completed

Conditions

Anesthesia

Treatments

Drug: Dexamethasone
Drug: Mepivicaine

Study type

Interventional

Funder types

Other

Identifiers

NCT00802009
08-0896-B

Details and patient eligibility

About

Patients undergoing surgery of the hand often are treated with a nerve block in the shoulder/neck area that provides anesthesia/numbing during surgery. Nerve blocks usually last for a few hours after surgery and provide pain relief for this period. It may be possible to extend the duration of anesthesia by using a steroid, which has anti-inflammtory properties. This study will compare the duration of the nerve block when dexamethasone (steroid) is added to the anesthetic injected around the nerve.

Enrollment

44 estimated patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Patients having unilateral hand or forearm surgery under Supraclavicular brachial plexus blockade.
  2. ASA I-III
  3. Age 18-60
  4. BMI < 35

Exclusion criteria

  1. Patients with a known history of hypersensitivity to local anesthetics and dexamethasone.
  2. Contra-indication to regional anesthesia/ supraclavicular brachial plexus blockade e.g. bleeding diathesis, coagulopathy.
  3. Peripheral neuropathy.
  4. Peptic ulcer disease.
  5. Diabetes Mellitus.
  6. Inability to give informed consent.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

44 participants in 2 patient groups

1
Experimental group
Description:
Dexamethasone 8mg added to routine local anesthetic during brachial plexus blockade.
Treatment:
Drug: Dexamethasone
Drug: Mepivicaine
2
Active Comparator group
Description:
Routine anesthetic solution (30 cc 1.5% mepivicaine) used during brachial plexus blockade.
Treatment:
Drug: Mepivicaine

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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