Evaluation of Collagen-based Medical Device Treatment Combined With Physiotherapy in Subjects With Achilles Tendinopathy. Multicenter Randomized Clinical Investigation; AKITENMED STUDY.

Status: Recruiting
Location: See location...
Intervention Type: Other, Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Achilles tendinopathy is a condition characterized by inflammation of the Achilles tendon. Achilles tendinopathies are classified into insertional tendinitis and noninsertional tendinitis. Insertional tendinitis involves the lower part of the tendon, where the tendon inserts at the level of the calcaneus, and can affect even patients who are not particularly athletically active. Noninsertional tendinitis occurs when the fibers in the middle portion of the tendon are affected, affects young and athletic people the most, and has a high incidence (30-50%) in middle-aged individuals. Considering that there are no strong evidence-based guidelines in the area of treatment of achilles tendinopathy, the aim of this research project is to understand through a multicenter, randomized clinical investigation the impact of treatment with a porcine collagen-based medical device administered in the peri-tendon area in combination with physiotherapy on pain reduction and functional improvement of the investigated tendon.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 70
Healthy Volunteers: f
View:

• Male and female subjects aged 18 to 70 years;

• Subjects with tendon pain for not more than 24 weeks;

• Subjects with clinically diagnosed and ultrasonographically confirmed insertional/noninsertional/mystic tendinopathy;

• Subjects with a VISA A score between 50 and 75;

• VAS ≥ 5;

• Subjects able to understand and answer the SF12 questionnaire;

• Subjects able to understand and sign the informed consent.

Locations
Other Locations
Italy
U.O.C. Medicina Fisica e Riabilitativa dell'AOU Policlinico Umberto I°
RECRUITING
Roma
Contact Information
Primary
Miranda MV Vincenzo, Dr
v.miranda@guna.it
3351311917
Backup
Laarej Kamilia, Dr
k.laarej@guna.it
0228018359
Time Frame
Start Date: 2022-06-13
Estimated Completion Date: 2026-01-13
Participants
Target number of participants: 72
Treatments
Experimental: MD-Tissue Medical Device
Group A which, alongside physiotherapy (eccentric strengthening protocol) will receive MD-Tissue Collagen Medical Device.
Other: Eccentric strengthening protocol
Group B who will only perform physiotherapy (eccentric strengthening protocol).
Related Therapeutic Areas
Sponsors
Leads: Guna S.p.a

This content was sourced from clinicaltrials.gov