Overview

A Comparison of Ropivacaine Alone Versus Combination of Dexamethasone and Clonidine for Block

Status:
Completed
Trial end date:
2016-08-20
Target enrollment:
0
Participant gender:
All
Summary
The aim of this randomized, observer-blinded study is to evaluate the postoperative analgesic efficacy of adding dexamethasone and clonidine to ropivacaine in supraclavicular nerve block. The investigators hypothesized that addition of dexamethasone and clonidine to ropivacaine would prolong the duration of analgesia in supraclavicular nerve block compared with ropivacaine alone.
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
University of Texas Southwestern Medical Center
Treatments:
BB 1101
Clonidine
Dexamethasone
Dexamethasone 21-phosphate
Dexamethasone acetate
Ropivacaine
Criteria
Inclusion Criteria:

- Men and women 18-80 years old

- Undergoing upper extremity surgery

- Receiving Supraclavicular block

- Receiving ropivacaine, ropivacaine adjuvants (dexamethasone, clonidine) for the
supraclavicular nerve block.

- Able to give Informed consent

Exclusion Criteria:

- Age less than 18 and greater than 80 years

- Inability to understand the study procedures

- Significant respiratory dysfunction

- Preexisting neurologic deficits

- Allergy to local anesthetics

- A bleeding diathesis or on anticoagulants

- Systemic glucocorticoid use

- Refuse to participate in the study