Total Hip Arthroplasty Clinical Trial
Official title:
Closed Suction Drain or Not After Total Hip Arthroplasty: A Randomized Controlled Trial
NCT number | NCT02845427 |
Other study ID # | AUHOR1 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | February 2016 |
Est. completion date | January 1, 2018 |
Verified date | February 2017 |
Source | Assiut University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Comparative randomised study to clarify which better to use or no use of closed suction drain system after total hip arthroplasty regarding amount of blood loss, need for blood transfusion, risk for superficial infection, ecchymosis, wound discharge, effect on early post-operative rehabilitation. Patients will be followed up for one month postoperative clinically (Harris Hip score system), laboratory (Hb level), and radiologically (A-P view plain x-ray of the hip).
Status | Completed |
Enrollment | 100 |
Est. completion date | January 1, 2018 |
Est. primary completion date | August 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Primary total hip arthroplasty (THA) Exclusion Criteria: - Revision cases - Uncontrolled bleeding tendency (prothrombin conc. Less than 70%) - History of deep venous thrombosis - Sever liver impairment (liver failure) - Sever renal impairment (S. creatinine more than 3) |
Country | Name | City | State |
---|---|---|---|
Egypt | Faculty of Medicine | Assiut |
Lead Sponsor | Collaborator |
---|---|
Assiut University |
Egypt,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | change in Hb level | preoperative and 24 hrs postoperative | ||
Secondary | amount of blood loss | upto 24 hrs postoperative | ||
Secondary | amount of blood transfusion | upto 24 hrs postoperative |
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