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Comparative Study of Minimally Invasive Surgical Approaches for Total Hip Arthroplasty

Comparative Study of Minimally Invasive Surgical Approaches for Total Hip Arthroplasty: a Biochemical, Imaging and Clinical Evaluation in the Early Postoperative Period

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04311125
Enrollment
90
Registered
2020-03-17
Start date
2020-04-01
Completion date
2022-05-01
Last updated
2020-03-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anterior Approach, Hip Arthropathy, Hip Osteoarthritis, Minimal Invasive, Tissue Injury

Brief summary

Total hip arthroplasty is a method of choice for treating advanced osteoarthritis of the hip and one of the most frequent orthopedic procedures. Of all hip surgical approaches described, the tendency for minimally invasive techniques has been dominated over the last few years due to faster patient mobilization, reduced postoperative pain and need for blood transfusion. Two of the most common approaches used for minimally invasive total hip arthroplasty are: AMIS anterior approach and mini-posterior approach, which is a modification of the standard posterior approach. The purpose of this study is the biochemical, imaging and clinical evaluation of the tissue damage caused by the above-mentioned techniques of minimally invasive total hip arthroplasty.

Interventions

PROCEDUREMini posterior approach Total Hip Replacement

Total hip replacement in patients suffering from hip osteoarthritis using the mini posterior approach

PROCEDUREAnterior approach total hip replacement without a traction table

Mini Anterior approach total hip replacement in patients suffering from hip osteoarthritis without the aid of a traction table

PROCEDUREAnterior approach total hip replacement with a traction table

Mini Anterior approach total hip replacement in patients suffering from hip osteoarthritis with the aid of a traction table

Sponsors

National and Kapodistrian University of Athens
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients that sign the Informed consent * Patients aged 18 years and over who are going to undergo primary total hip arthroplasty

Exclusion criteria

I. Active infection II. Previous hip operation in any leg III. Any kind of operation the past 3 months IV. Obesity (BMI, Body Mass Index \>30) V. Autoimmune diseases or myositis of any etiology VI. Active cancer

Design outcomes

Primary

MeasureTime frameDescription
Tissue damage changeChange from 6 to 24 and then 48 hours post-surgeryInvestigate and quantify at the biochemical level with all available biomarkers the extent of tissue damage caused during a hip arthroplasty between different hip surgical approaches.

Secondary

MeasureTime frameDescription
ImagingDay 30 after surgeryAll patients will be subjected to imaging with a hip MRI
Clinical Tests changeChange to clinical test from Day 2 to day 15 and then day 30 post-surgeryAll patients will be monitored postoperatively for the prescribed period and data will be recorded.

Countries

Greece

Contacts

Primary ContactVasileios Nikolaou
vassilios.nikolaou@gmail.com+306932543400

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026