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Trials / Completed

CompletedNCT01714297

Preoperative Versus Postoperative Start With Thromboprophylaxis in THA (Total Hip Arthroplasty)

A Prospective Randomized, Double Blind Study to Evaluate Safety and Effect With Pre Versus Postoperative Start of Thromboprophylaxis With Dalteparin

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
80 (actual)
Sponsor
Vestre Viken Hospital Trust · Academic / Other
Sex
All
Age
50 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to determine if there are differences in clinical events, i.e bleeding with associated morbidity, if thromboprophylaxis with LMWH (Low Molecular Weight Heparin) is initiated before or after surgery.

Conditions

Interventions

TypeNameDescription
DRUGdalteparin 5000 IU s.c.All patients receive injections with either 5000IU dalteparin or saline in the same volume the evening before surgery. All patients receive 5000IU dalteparin 6 hours after surgery and every day from day 2 until day 35.

Timeline

Start date
2008-01-01
Primary completion
2008-06-01
Completion
2009-04-01
First posted
2012-10-25
Last updated
2012-12-10

Locations

1 site across 1 country: Norway

Source: ClinicalTrials.gov record NCT01714297. Inclusion in this directory is not an endorsement.

Preoperative Versus Postoperative Start With Thromboprophylaxis in THA (Total Hip Arthroplasty) (NCT01714297) · Clinical Trials Directory