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Study to Evaluate Made-to-measure Compression Garments

B

BSN Medical

Status

Completed

Conditions

Lymphedema

Treatments

Device: JOBST® Confidence compression garments

Study type

Interventional

Funder types

Industry

Identifiers

Details and patient eligibility

About

The primary objective is to collect real-life data to evaluate the clinical performance and safety of innovative, made-to-measure, flat knitted, CE-marked compression garments for daytime treatment of leg or arm lymphedema (ISL stage I-II) in daily routine by analysing performance parameters and safety parameters reported during the investigation.

Full description

The secondary objective is to evaluate (1) patients' quality of life QoL before and after having tested JOBST Confidence and (2) patient satisfaction focussing on patient reported outcomes of previously worn garments and JOBST® Confidence by analysing patient questionnaires parameters completed at the beginning and in the end of the wearing period.

Enrollment

99 patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Signed Informed Consent Form
  2. Men, women or diverse aged 18 years or up to 70 years with full legal competence
  3. Patient is mentally and physically able to participate in the study
  4. Capability to understand the subject information and to provide conscious informed consent
  5. Capability and willingness to follow protocol requirements
  6. All female or diverse subjects of childbearing potential must agree to use a reliable method of contraception with a Pearl-Index of less than 1% per year when used consistently and correctly* (*such as hormone implants,injectables, combined oral contraceptives (combined gestagen-estrogen pills), some intra uterine devices (IUDs), surgically sterility (hysterectomy or tubal ligation), sexual abstinence or vasectomized partner for at least 4 weeks)
  7. Mild to moderate lymphedema of the lower and/or upper extremities (ISL stage I or II)
  8. Indication and possibility of treatment with a flat-knitted compression garment during the day
  9. Patients who are familiar with wearing compression garments
  10. Indicated Complete Decongestive Therapy Phase II (Maintenance phase)
  11. Willingness to wear the study product at least 5 days a week for at least 6 hours a day

Exclusion criteria

  1. Pregnant or lactating women or diverse subjects
  2. Alcohol abuse (mentioned by the patient and/or suspected by the investigator)
  3. Drug abuse (mentioned by the patient and/or suspected by the investigator)
  4. Patients who need a different compression class (higher or lower than CCL 2)
  5. Pronounced skin folds
  6. Pronounced shape distortions
  7. cG (lymphatic measure of the thigh) >90 cm for AG stocking
  8. Indicated Complete Decongestive Therapy Phase I
  9. Known allergy or intolerance to one or more components of the product
  10. Advanced arterial insufficiency including ischemia
  11. Uncontrolled congestive heart failure
  12. Untreated septic phlebitis
  13. Phlegmasia coerulea dolens
  14. Immobility (confinement to bed).
  15. Conditions in which increased venous and lymphatic return is not desired.
  16. Weeping dermatosis
  17. Cutaneous infections
  18. Severely compromised skin sensibility and impaired sensitivity of the limb
  19. Advanced peripheral neuropathy
  20. Rheumatoid arthritis
  21. Complex regional pain syndrome (CRPS, M. Sudeck)
  22. Malignant lymphedema
  23. Gangrene
  24. Sponsors or manufacturers staff
  25. Open wounds in the test area
  26. Diuretics, except low doses for treatment of hypertension (≤ 12.5 mg Hydrochlorothiazide)
  27. Nephrotic syndrome

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

99 participants in 1 patient group

JOBST® Confidence compression garments
Experimental group
Description:
The CE-marked class I medical devices JOBST® Confidence compression garments for lower and upper extremities will be tested under routine conditions according to their selected intended use. Subjects will be treated with either thigh-high compression stockings (AG) or arm compression garments without hand part (CG1), depending on their indication.
Treatment:
Device: JOBST® Confidence compression garments

Trial contacts and locations

4

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Data sourced from clinicaltrials.gov

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