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Lipid Peroxidation and Options Antioxidant Therapy for Secondary Lymphedema of the Lower Extremities

Primary Purpose

Lower Extremity Lymphedema

Status
Completed
Phase
Phase 4
Locations
Russian Federation
Study Type
Interventional
Intervention
Micronised purified flavonoid fraction (diosmin+flavonoids expressed as hesperidin)
Tocopherol
Elastic compression
Sponsored by
Ryazan State Medical University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Lower Extremity Lymphedema focused on measuring endothelial dysfunction, secondary lymphedema of the lower extremities, antioxidants, micronized purified flavonoid fraction

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesAccepts Healthy Volunteers

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.

Sites / Locations

  • Ryazan State Medical University

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Other

No Intervention

Arm Label

Tocopherol

Micronised purified flavonoid fraction

Elastic compression

Healthy volunteers

Arm Description

patients with lower limb lymphedema who will receive conservative therapy with elastic compression and an antioxidant (Tocopherol-400 IU/day) - 90 days

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 - 90 days

patients with lower limb lymphedema who will be treated with elastic compression - 90 days

healthy volunteers with no history or clinical signs of venous or lymphatic disease - 90 days

Outcomes

Primary Outcome Measures

The malleolar volume of the limb
The circumference at the level of the narrowest part of the lower leg, measured in centimeters
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
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
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
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
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.

Secondary Outcome Measures

Full Information

First Posted
April 18, 2020
Last Updated
August 3, 2022
Sponsor
Ryazan State Medical University
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1. Study Identification

Unique Protocol Identification Number
NCT04360889
Brief Title
Lipid Peroxidation and Options Antioxidant Therapy for Secondary Lymphedema of the Lower Extremities
Official Title
Lipid Peroxidation and Options Antioxidant Therapy for Secondary Lymphedema of the Lower Extremities
Study Type
Interventional

2. Study Status

Record Verification Date
August 2022
Overall Recruitment Status
Completed
Study Start Date
September 1, 2019 (Actual)
Primary Completion Date
August 3, 2022 (Actual)
Study Completion Date
August 3, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Ryazan State Medical University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief 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.
Detailed Description
Research methods: Physical examination; 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). Lower limb venous sonography with a linear 5-13 MHz probe; Patient questionnaire using a Russian-language version of the Quality of life questionnaire "SF-36 Health Status Survey"

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lower Extremity Lymphedema
Keywords
endothelial dysfunction, secondary lymphedema of the lower extremities, antioxidants, micronized purified flavonoid fraction

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
120 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Tocopherol
Arm Type
Experimental
Arm Description
patients with lower limb lymphedema who will receive conservative therapy with elastic compression and an antioxidant (Tocopherol-400 IU/day) - 90 days
Arm Title
Micronised purified flavonoid fraction
Arm Type
Experimental
Arm Description
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 - 90 days
Arm Title
Elastic compression
Arm Type
Other
Arm Description
patients with lower limb lymphedema who will be treated with elastic compression - 90 days
Arm Title
Healthy volunteers
Arm Type
No Intervention
Arm Description
healthy volunteers with no history or clinical signs of venous or lymphatic disease - 90 days
Intervention Type
Drug
Intervention Name(s)
Micronised purified flavonoid fraction (diosmin+flavonoids expressed as hesperidin)
Intervention Description
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
Intervention Type
Drug
Intervention Name(s)
Tocopherol
Intervention Description
patients with lower limb lymphedema receiving conservative therapy (elastic compression, to which are added preparations with antioxidant endotheliotropic activity (Tocopherol-400 IU/day)
Intervention Type
Other
Intervention Name(s)
Elastic compression
Intervention Description
patients with lower limb lymphedema receiving conservative therapy that includes only the use of elastic compression
Primary Outcome Measure Information:
Title
The malleolar volume of the limb
Description
The circumference at the level of the narrowest part of the lower leg, measured in centimeters
Time Frame
90 days
Title
The Level Of Catalase
Description
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
Time Frame
90 days
Title
The Level Of Superoxide Dismutase
Description
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
Time Frame
90 days
Title
The Level Of Glutathione Peroxidase
Description
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
Time Frame
90 days
Title
The level of Malondialdehyde
Description
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
Time Frame
90 days
Title
Quality of life indicators: questionnaire
Description
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.
Time Frame
90 days

10. Eligibility

Sex
All
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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.
Facility Information:
Facility Name
Ryazan State Medical University
City
Ryazan'
ZIP/Postal Code
390026
Country
Russian Federation

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Lipid Peroxidation and Options Antioxidant Therapy for Secondary Lymphedema of the Lower Extremities

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