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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00921908
Other study ID # H-A-2008-028
Secondary ID
Status Completed
Phase N/A
First received June 16, 2009
Last updated June 16, 2009
Start date October 2008
Est. completion date June 2009

Study information

Verified date June 2009
Source Hvidovre University Hospital
Contact n/a
Is FDA regulated No
Health authority Denmark: The Regional Committee on Biomedical Research Ethics
Study type Observational

Clinical Trial Summary

Postoperative administration of local anesthetics is effective for postoperative pain management across surgical specialties but the optimal type of catheter (single, few or multiholed catheters) has not been determined.

This study investigates wound spread of a radioactive isotope (technetium) administered in different types of catheters after total hip arthroplasty.


Recruitment information / eligibility

Status Completed
Enrollment 16
Est. completion date June 2009
Est. primary completion date June 2009
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- operation with total hip arthroplasty

Exclusion Criteria:

- allergies to drugs administered

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Other:
2 mBq radioactive technetium diluted in 20 mL saline


Locations

Country Name City State
Denmark Hvidovre University Hospital Hvidovre

Sponsors (1)

Lead Sponsor Collaborator
Hvidovre University Hospital

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary wound spread area of radioactive isotope
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