Observational study to evaluate trochanteric fractures and wound healing disorders in patients with hip TEP implants using the AMIS ( anterior minimal invasive surgery) DAA ( direct anterior approach )

Recruiting

• Conditions: M16.1; T81.8; Other primary coxarthrosis; Other complications of procedures, not elsewhere classified

• Registration Number: DRKS00009603
• Lead Sponsor: ACURA Kliniken Albstadt GmbH

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2016-02-15
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 150

Inclusion Criteria

Coxarthrosis
- Male and female patients between 30 an 80 years of Age
Patients who had undergone a programmed total hip replacemenet surgery in AMIS DAA and had a 4 week postoperative medical Observation
-Compliance with the ordered postoperative medical Treatment
- Agreement in written form of the participating Person
- full contractual capability

Exclusion Criteria

- Hip replacement after hip fracture
- Intolerance to plaster
- Addiction oder other diseases that don´t allow the patient to follow the postoperative regime
- Oral anticoagulation in medical history
- Corticoide treatment or other immunsupressive treatment
- local skin abnormalities

Study & Design

• Study Type: observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Frequency of intraoperative and perioperative trochanter avulsion fractures and trochanter infraction<br><br>Frequency of wound healing disorders following the implantation of total hip endoprostheses through minimally invasive access<br><br>The endpoint is the last clinical and if necessary the last radiological examination at the end of the rehabilitation programme about 4 weeks after surgery.

Secondary Outcome Measures

Name	Time	Method
Incidence of revision due to seromas/hematomas<br>Incidence of revision due to fractures<br>Incidence of revision due to wound healing disorders<br>Incidence of revision in total<br><br>The endpoint is the last clinical and if necessary the last radiological examination at the end of the rehabilitation programme about 4 weeks after surgery.