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Evaluation of the Duration of Bupivacaine Spinal Block in Orthopedic Procedures With and Without Epinephrine Wash

Medical University of South Carolina (MUSC) logo

Medical University of South Carolina (MUSC)

Status

Completed

Conditions

Arthropathy of Hip
Arthropathy of Knee

Treatments

Drug: EPI75 group
Drug: EPI50 group
Drug: EPI100 group
Drug: Bupivacaine Only
Drug: EPI25

Study type

Interventional

Funder types

Other

Identifiers

NCT02619409
Pro00039232

Details and patient eligibility

About

Bupivacaine spinal is commonly performed as the primary anesthetic for orthopedic procedures. In some cases the duration of the block is inadequate. An epinephrine wash is sometimes performed to prolong the duration of the block. The epinephrine wash may prolong the duration of the block, and if it does, to what extent?

Enrollment

30 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 18 years of age or older
  • Patients scheduled for total hip or knee replacement

Exclusion criteria

  • Patients taking anticoagulation
  • Infection at or near the intended needle insertion site
  • Patients with sacral decubitus ulcer at or near the intended needle insertion site aortic stenosis
  • Complex spine anatomy
  • ASA class greater than III
  • Failed SAB as determined by the staff anesthesiologist

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

30 participants in 5 patient groups, including a placebo group

Bupivacaine Only
Placebo Comparator group
Description:
The bupivacaine only group will receive bupivacaine 0.5% 3cc plus sterile saline 0.1cc.
Treatment:
Drug: Bupivacaine Only
EPI25 group
Active Comparator group
Description:
The EPI25 group will receive bupivacaine 0.5% 3cc, epinephrine 1:1000 0.025cc, and sterile saline 0.075cc.
Treatment:
Drug: EPI25
EPI50 group
Active Comparator group
Description:
The EPI50 group will receive bupivacaine 0.5% 3cc, epinephrine 1:1000 0.05cc, and sterile saline 0.05cc.
Treatment:
Drug: EPI50 group
EPI75 group
Active Comparator group
Description:
The EPI75 group will receive bupivacaine 0.5% 3cc, epinephrine 1:1000 0.075 cc, and sterile saline 0.025%.
Treatment:
Drug: EPI75 group
EPI100 group
Active Comparator group
Description:
The EPI100 group will receive bupivacaine 0.5% 3cc, and epinephrine 1:1000 0.1cc
Treatment:
Drug: EPI100 group

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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