Knee surgery drain debate: new study compares blood loss with and without drain
NCT ID NCT07494708
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study looked at whether placing a drain after knee replacement surgery affects how much hemoglobin drops and whether patients need a blood transfusion. 102 patients were randomly assigned to get a drain or not. The goal is to see if drains help or hurt in terms of blood loss. Results could help guide standard practice.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Closed suction drain insertion
- What this could lead to
- If this study shows clear differences, it could help surgeons decide whether to use a drain after knee replacement, potentially reducing blood loss and transfusion needs.
- What could go wrong
- This is a small, completed study (102 patients) that only measures short-term outcomes. Results may not apply to all patients or settings, and the best approach may still depend on individual factors.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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102 people
The number who actually took part.
- Started
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Aug 2025
- Finished
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Jan 2026
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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50 to 80 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age between 50 and 80 years. * Both male and female patients. * Diagnosed with: * Primary knee osteoarthritis. * Rheumatoid arthritis. * Arthritis following trauma. * Osteonecrosis, or avascular necrosis. * Unilateral primary total knee arthroplasty (TKA) is necessary due to severe knee pain, stiffness, and non-responsiveness to conservative treatment. * Patients with a Knee Society Score (KSS) of ≤60 are considered to have functional limitations, which are characterized as a severe impairment in activities of daily living (ADLs) related to knee disease. * Preoperative hemoglobin ≥10 g/dL to ensure comparable baseline hemoglobin levels across groups. * BMI between 18.5 and 35 kg/m² to exclude extremes of underweight or morbid obesity. Exclusion Criteria: * Patients undergoing revision TKA due to implant failure, infection, or periprosthetic fractures. * Individuals with aberrant coagulation parameters (INR \>1.5, extended PT/aPTT) or inherited or acquired bleeding diseases (such as hemophilia or von Willebrand disease). * Patients receiving antiplatelet therapy (ticagrelor, clopidogrel) or long-term anticoagulants (warfarin, DOACs) within seven days of surgery. * Individuals with sickle cell disease, thalassemia, or chronic anemia (Hb \<10 g/dL). * Individuals with severe COPD, pulmonary hypertension, NYHA Class III or IV heart failure, or a history of DVT/PE within the last six months. * Severe chronic kidney disease (CKD) stage 4/5 (eGFR \<30 mL/min/1.73m²) or severe hepatic dysfunction (Child-Pugh Class C, AST/ALT \>3×normal, bilirubin \>2 mg/dL). * Patients with active systemic infections (sepsis, tuberculosis, HIV/AIDS, hepatitis B/C, osteomyelitis). * Patients with a history of thromboembolic events (DVT/PE/stroke within 12 months) or contraindications to tranexamic acid (TXA). * Pregnant or lactating women.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Shifa International Hospital, Islamabad
Islamabad, Fedral, 44000, Pakistan
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