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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03160781
Other study ID # UCA-01-EC/13/ART
Secondary ID
Status Completed
Phase Phase 2
First received May 17, 2017
Last updated May 18, 2017
Start date January 28, 2014
Est. completion date January 10, 2015

Study information

Verified date May 2017
Source Unidad de Cirugía Artroscópica
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study was to assess a novel approach to treating severe knee osteoarthritis by targeting synovialmembrane, superficial articular cartilage, synovial fluid, and subchondral bone by combining intra-articular injections and intraosseous infiltrations of platelet rich plasma.This study explored a new strategy consisting of intraosseous infiltrations of platelet rich plasma into the subchondral bone in combination with the conventional intra-articular injection in order to tackle several knee joint tissues simultaneously.


Recruitment information / eligibility

Status Completed
Enrollment 19
Est. completion date January 10, 2015
Est. primary completion date January 10, 2015
Accepts healthy volunteers No
Gender All
Age group 40 Years to 77 Years
Eligibility Inclusion Criteria:

- Patients of both sexes aged 40 to 77 years.

- Predominant internal tibiofemoral knee osteoarthritis.

- Joint pain above 2.5 VAS points.

- Radiographic severity degrees 3 and 4 according to Ahlbäck scale.

- Values of body mass index between 20 and 33.

- Possibility for observation during the follow-up period.

Exclusion Criteria:

- Bilateral knee osteoarthritis which requires infiltration in both knees.

- Values of body mass index > 33.

- Polyarticular disease diagnosed.

- Severe mechanical deformity (diaphyseal varus of 4° and valgus of 16°).

- Arthroscopy in the last year prior to treatment.

- Intra-articular infiltration of hyaluronic acid in the past 6 months.

- Systemic autoimmune rheumatic disease (connective tissue diseases and systemic necrotizing vasculitis).

- Poorly controlled diabetes mellitus (glycosylated hemoglobin above 9%).

- Blood disorders (thrombopathy, thrombocytopenia, and anemia with Hb < 9).

- Undergoing immunosuppressive therapy and/or warfarin.

- Treatment with corticosteroids during the 6 months prior to inclusion in the study.

Study Design


Related Conditions & MeSH terms


Intervention

Biological:
Platelet Rich Plasma
Combination of Intraosseous and Intraarticular Infiltration of Platelet Rich Plasma

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Unidad de Cirugía Artroscópica

Outcome

Type Measure Description Time frame Safety issue
Primary Pain according to KOOS scale at 6 months after treatment Pain according to KOOS scale 6 months
Secondary Symptoms according to KOOS scale at 6 months after treatment According to KOOS scale 6 months
Secondary Function according to KOOS scale at 6 months after treatment According to KOOS scale 6 months
Secondary Sport Activity according to KOOS scale at 6 months after treatment According to KOOS scale 6 months
Secondary QoL according to KOOS scale at 6 months after treatment According to KOOS scale 6 months
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