Impact of surgical methods on bleeding after hip replacement surgery
Effect of Surgical Approach on Postoperative Bleeding in Patients Undergoing Hip Arthroplasty: Anterior Vs. Posterolateral Route
This study is testing whether different surgical methods for hip replacement can reduce bleeding and pain, and help patients recover faster.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 50 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio Academic / other |
| Locations | 1 site (Milan) |
| Trial ID | NCT06308003 on ClinicalTrials.gov |
What this trial studies
This observational study aims to evaluate the effects of different surgical approaches on postoperative bleeding, pain, and hospital stay duration in adult patients undergoing hip arthroplasty for hip arthropathy. Patients will be assessed preoperatively and at various postoperative intervals to measure hemoglobin levels, pain using a VAS questionnaire, and any adverse events. The study hypothesizes that certain surgical techniques may lead to less bleeding and pain, potentially reducing recovery time. The primary outcome will focus on blood loss measured by hemoglobin levels on the third postoperative day.
Who should consider this trial
Good fit: Ideal candidates are adult patients with hip arthropathy who are scheduled for hip arthroplasty surgery.
Not a fit: Patients who are minors, pregnant, have a BMI of 30 or higher, or have had prior hip surgery may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved surgical techniques that minimize postoperative bleeding and pain, enhancing recovery for hip arthroplasty patients.
How similar studies have performed: While similar studies have explored surgical approaches in hip arthroplasty, this specific observational study focuses on the comparative outcomes of bleeding and pain, making it a novel investigation.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * adult patients with coxarthrosis who are candidates for surgery hip arthroplasty * Signing of the Informed Consent and consent to collaborate in all study procedures. Exclusion Criteria: * Minors * Pregnant women (self-declaration) * patients with BMI ≥ 30 * Non-acceptance of informed consent * Patients with prior unilateral hip reconstructive surgery or Contralateral
Where this trial is running
Milan
- Istituto Clinico San Siro — Milan, Italy (Recruiting)
Study contacts
- Principal investigator: Alberto Ventura — Ospedale Galeazzi-Sant'Ambrogio
- Study coordinator: Elena Cittera
- Email: elena.cittera@grupposandonato.it
- Phone: 0283502224
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.