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Pain Management After Shoulder Prosthesis: A Clinical Trial of Nerve Block and Local Infiltration

NCT01362075 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 74

Last updated 2014-08-08

No results posted yet for this study

Summary

The purpose of this study is to determine the efficacy of local infiltration analgesia as compared to 48-hour interscalene block in treating pain after shoulder arthroplasty. The investigators hypothesize a reduced pain score and use of supplemental analgesic medication during the first three postoperative days using local infiltration analgesia.

Conditions

  • Pain, Postoperative

Interventions

PROCEDURE

Local infiltration analgesia

150 ml ropivacaine, of which 100 ml is with adrenalin

PROCEDURE

Interscalene catheter

7 ml ropivacaine interscalene block via catheter, subsequently given 5 ml/h and possibility of 5 ml bolus for the first 48 hours.

Sponsors & Collaborators

  • Horsens Hospital

    lead OTHER

  • University of Aarhus

    collaborator OTHER

  • Aarhus University Hospital

    collaborator OTHER

  • The Hede Nielsen Family Foundation

    collaborator OTHER

  • Central Denmark Region

    collaborator OTHER

  • The Danish Rheumatism Association

    collaborator OTHER

Principal Investigators

  • Karen T Bjørnholdt, MD · Horsens Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
90 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-07-31
Primary Completion
2014-07-31
Completion
2014-10-31

Countries

  • Denmark

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01362075 on ClinicalTrials.gov