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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 )

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 ) - TroWAd

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00009603
Enrollment
150
Registered
2016-02-15
Start date
2016-02-01
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

M16.1 T81.8

Interventions

Group 1: The observational study seeks to evaluate retrospective data of coxarthrosis patients with hip TEP implants using AMIS DAA. The patient group is made up of routine treatment cases at our clin

Sponsors

ACURA Kliniken Albstadt GmbH
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 80 Years

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
Frequency of intraoperative and perioperative trochanter avulsion fractures and trochanter infraction Frequency of wound healing disorders following the implantation of total hip endoprostheses through minimally invasive access 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

MeasureTime frame
Incidence of revision due to seromas/hematomas Incidence of revision due to fractures Incidence of revision due to wound healing disorders Incidence of revision in total 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.

Countries

Germany

Contacts

Public ContactEmese Scholl

ACURA Kliniken Albstadt GmbH

emese.scholl@acura-kliniken-albstadt.com07431-1692003

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026