Achilles tendon surgery - functionality after treatment of infection - a preliminary study with query of patient-reported outcome data (PROM).

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00031755

Enrollment

Registered

2023-04-27

Start date

2021-06-01

Completion date

Unknown

Last updated

2026-06-01

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

Conditions

S86.0

Interventions

Group 1: Achilles tendon surgery

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Index procedure performed by 12/31/2019. Documented performance of a partial or complete Achilles tendon resection at BGKH for any indication without performing a secondary plastic. Presentation of a signed declaration of consent for the scientific evaluation of patient data assigned to the treatment in question.

Exclusion criteria

Exclusion criteria: Patients who do not have an independently signed consent for data use (e.g., signature by relatives due to impaired cognitive function).

Design outcomes

Primary

Measure	Time frame
achieved function of the Achilles tendon	—

Secondary

Measure	Time frame
It is not a controlled study or a regulatory trial. Therefore, primary or secondary outcome measures in the conventional sense do not exist. A treatment cohort of a hospital over a period of 10 years is considered. The aim is to evaluate the maximum possible number of data sets, which are limited only by the inclusion/exclusion factors. While primarily the achieved function of the Achilles tendon is put in relation to the other recorded items, a description of the study population as well as a detailed evaluation of the recorded complications and the description of the factors influencing the occurrence of a complication are also secondary. factors influencing the occurrence of a complication.	—

Measure

Time frame

It is not a controlled study or a regulatory trial. Therefore, primary or secondary outcome measures in the conventional sense do not exist. A treatment cohort of a hospital over a period of 10 years is considered. The aim is to evaluate the maximum possible number of data sets, which are limited only by the inclusion/exclusion factors. While primarily the achieved function of the Achilles tendon is put in relation to the other recorded items, a description of the study population as well as a detailed evaluation of the recorded complications and the description of the factors influencing the occurrence of a complication are also secondary. factors influencing the occurrence of a complication.

—

Countries

Germany

Contacts

Public ContactArndt-Peter Schulz

BG Klinikum Hamburg

schulz@biomechatronics.de+494073061616

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Jun 11, 2026