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The Use of Bupivacaine and Ropivacaine for Sciatic Nerve Block

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Northwestern University

Status and phase

Completed
Phase 4

Conditions

The Duration of Motor Block May Vary Between 12-36 Hrs

Treatments

Drug: Ropivacaine
Drug: Bupivacaine

Study type

Interventional

Funder types

Other

Identifiers

NCT01272921
STU00035380

Details and patient eligibility

About

The duration of motor block for infragluteal parabiceps sciatic nerve block following total knee replacement may vary between 12-36 hrs depending on the amount of local anesthetic given.

Enrollment

142 patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult patients (>18 years of age) who are undergoing elective total knee arthroplasty will be included in the study.

Exclusion criteria

  • Exclusion criteria for the study are patient refusal to be included in the study, contraindications to regional anesthesia, history of allergy to amide local anesthetics, the presence of a progressive neurological deficit, the presence of coagulopathy or infection, or pregnancy

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

142 participants in 2 patient groups

Bupivacaine
Active Comparator group
Description:
Varying does to determine duration of analgesia following a sciatic nerve block
Treatment:
Drug: Bupivacaine
Ropivacaine
Active Comparator group
Description:
Varying does to determine duration of analgesia following a sciatic nerve block
Treatment:
Drug: Ropivacaine

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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