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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04360889
Other study ID # MDA-1
Secondary ID
Status Completed
Phase Phase 4
First received
Last updated
Start date September 1, 2019
Est. completion date August 3, 2022

Study information

Verified date August 2022
Source Ryazan State Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

A single-center, open, prospective, randomized, controlled clinical trial will include 120 patients with lower limb lymphedema who undergo treatment in an office-based vascular lab at the Ryazan regional clinical cardiology dispensary, Ryazan, Russia. The patients will be recruited by the staff of the Department of cardiovascular, endovascular, operative surgery, and topographic anatomy, Ryazan state I.P. Pavlov medical university, Russia. The study will include patients who meet the inclusion criteria and do not meet the exclusion criteria. Patients will be divided into 4 groups, 30 subjects each. Group 1-patients with lower limb lymphedema who will receive conservative therapy with elastic compression and an antioxidant (Tocopherol-400 IU/day); Group 2-patients with lower limb lymphedema who will receive conservative therapy with Micronised purified flavonoid fraction (diosmin+flavonoids expressed as hesperidin)-1000mg/day) in addition to elastic compression; Group 3-patients with lower limb lymphedema who will be treated with elastic compression; Group 4- healthy volunteers with no history or clinical signs of venous or lymphatic disease; The duration of this study for each subject will be a maximum of 90 days. Pre-screening and screening will involve 200 subjects with a total of 120 subjects who will be randomized into the study. Peripheral blood samples will be collected to evaluate the activity of biochemical markers of endothelial function; the quality of life will also be assessed.


Description:

Research methods: 1. Physical examination; 2. peripheral blood sampling (assessment of the concentration of the markers of endothelial dysfunction, including malondialdehyde (MDA), superoxide dismutase (SD), catalase( CAT), glutathione peroxidase (GP). MDA concentration will be determined with a competitive enzyme immunoassay (ELISA), which will be performed using a General MDA assessment kit (manufacturer: USCN Life Science Inc. US-CEA597GE). CAT concentration will be determined using a competitive enzyme immunoassay (ELISA), which will be performed with a kit for quantitative in vitro assessment of catalase (manufacturer: USCN Life Science Inc. US-SEC418Hu). GP concentration will be determined with a competitive enzyme immunoassay (ELISA), which will be performed using a glutathione peroxidase quantification set (abfrontier supplier, Republic of Korea - LF- EK0110). SOD concentration will be determined using a competitive enzyme immunoassay (ELISA), which will be performed using a total superoxide dismutase detection kit (supplier Cayman Chemical Company, US - 706002). 3. Lower limb venous sonography with a linear 5-13 MHz probe; 4. Patient questionnaire using a Russian-language version of the Quality of life questionnaire "SF-36 Health Status Survey"


Recruitment information / eligibility

Status Completed
Enrollment 120
Est. completion date August 3, 2022
Est. primary completion date August 3, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Secondary lymphedema of the lower extremities - Signed Informed Consent Form Exclusion Criteria: - varicose veins of the lower extremities, - deep vein thrombosis, - post-thrombotic disease, - obliterating - atherosclerosis of the lower limb arteries, - pregnancy, - lactation, - cancer, - acute violation of cerebral circulation in the anamnesis, - trophic lesions of the skin of the lower extremities, - diabetes mellitus - an infectious disease with a history of three months prior to inclusion in the study, - heart failure, - kidney failure, - pulmonary insufficiency.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Micronised purified flavonoid fraction (diosmin+flavonoids expressed as hesperidin)
Micronised purified flavonoid fraction (diosmin+flavonoids expressed as hesperidin) is prescribed at a dose of 1000 mg / day Tocopherol is prescribed at a dose of 400 ME/ day
Tocopherol
patients with lower limb lymphedema receiving conservative therapy (elastic compression, to which are added preparations with antioxidant endotheliotropic activity (Tocopherol-400 IU/day)
Other:
Elastic compression
patients with lower limb lymphedema receiving conservative therapy that includes only the use of elastic compression

Locations

Country Name City State
Russian Federation Ryazan State Medical University Ryazan'

Sponsors (1)

Lead Sponsor Collaborator
Ryazan State Medical University

Country where clinical trial is conducted

Russian Federation, 

Outcome

Type Measure Description Time frame Safety issue
Primary The malleolar volume of the limb The circumference at the level of the narrowest part of the lower leg, measured in centimeters 90 days
Primary The Level Of Catalase Biochemical indicator of the functional state of the endothelium. Catalase concentration will be determined using a competitive enzyme immunoassay (ELISA), which will be performed with a kit for quantitative in vitro assessment of catalase (manufacturer: USCN Life Science Inc. US-SEC418Hu). Unit of measurement ng / ml 90 days
Primary The Level Of Superoxide Dismutase Biochemical indicator of the functional state of the endothelium. Superoxide Dismutase concentration will be determined using a competitive enzyme immunoassay (ELISA), which will be performed using a total superoxide dismutase detection kit (supplier Cayman Chemical Company, US - 706002). Unit of measurement UI / ml 90 days
Primary The Level Of Glutathione Peroxidase Biochemical indicator of the functional state of the endothelium. Glutathione Peroxidase concentration will be determined with a competitive enzyme immunoassay (ELISA), which will be performed using a glutathione peroxidase quantification set (abfrontier supplier, Republic of Korea - LF- EK0110). Unit of measurement ng / ml 90 days
Primary The level of Malondialdehyde Biochemical indicator of the functional state of the endothelium. Malondialdehyde concentration will be determined with a competitive enzyme immunoassay (ELISA), which will be performed using a General MDA assessment kit (manufacturer: USCN Life Science Inc. US-CEA597GE). Unit of measurement ng / ml 90 days
Primary Quality of life indicators: questionnaire Patient questionnaire using a Russian-language version of the Quality of life questionnaire "Short Form-36 Health Status Survey". 8 indicators. Indicator from 0 to 100. Higher scores mean a better outcome. 90 days
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