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Local Anesthetic Infiltration and Infusion for Pain Control After Hip Replacement

T

Trinity Health Of New England

Status

Completed

Conditions

Osteoarthritis

Treatments

Procedure: Normal Saline
Procedure: Ropivacaine infiltration and saline infusion.
Procedure: Ropivacaine infiltration and infusion.

Study type

Interventional

Funder types

Other

Identifiers

NCT01409278
09-07-002

Details and patient eligibility

About

The purpose of this study is to examine three different ways to control pain after hip replacement:

  1. One time injection of ropivacaine before wound closure
  2. One time injection of ropivacaine before wound closure plus slow release of ropivacaine via catheter for 48 hours
  3. Standard practice of patient controlled pump

Enrollment

105 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • total knee replacement

Exclusion criteria

  • History of neurological disease, diabetes, pregnancy, allergy to local anesthetic solutions chronic narcotic use ability to consent

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

105 participants in 3 patient groups, including a placebo group

Ropivacaine infiltration and infusion.
Experimental group
Description:
Ropivicaine infiltration followed by continuous ropivicaine infusion for 48 hours.
Treatment:
Procedure: Ropivacaine infiltration and infusion.
Ropivacaine and Saline
Experimental group
Description:
Ropivicaine infiltration followed by normal saline infusion.
Treatment:
Procedure: Ropivacaine infiltration and saline infusion.
Saline infiltration and infusion.
Placebo Comparator group
Description:
Normal saline infiltration followed by saline infusion.
Treatment:
Procedure: Normal Saline

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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