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The effect of the use of Infrared Radiation Station on patients with Limb Venous Úlcers

The effect of the use of Infrared Radiation Station on patients with Limb Venous Úlcers: randomized clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-8c7xzn
Enrollment
Unknown
Registered
2018-10-22
Start date
2016-10-17
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Wound Healing, Varicose Ulcer

Interventions

Experimental group: 12 subjects with venous ulcers received bands with infrared emitting ceramic material,cover dressings with fatty acids Placebo group: 12 subjects with venous ulcers received bands
Radiation
Other
Q65.050

Sponsors

Universidade Regional do Noroeste do Estado do Rio Grande do Sul - UNIJUI
Lead Sponsor
Universidade do Sul de Santa Catarina
Collaborator

Eligibility

Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: to be over 18 years of age; Present medical diagnosis of chronic venous insufficiency recorded in the medical record; Being in medical follow-up at the Vascular Surgery Service of the Charity Hospital of Ijuí; No ulcer with arterial, neuropathic or mixed etiology.

Exclusion criteria

Exclusion criteria: to present irregularities in the frequency of attendance at the consultations; Discontinuity and nonadherence in ulcer treatment; Infected ulcer; Ischemia in the affected limb.

Design outcomes

Primary

MeasureTime frame
Reduction of at least 1 cm in the size of the venous ulcer, determined by measuring the ulcer by means of a 30 cm ruler comparing the pre-intervention evaluation and after 90 days of intervention.

Secondary

MeasureTime frame
Improvement of the score of at least 0.5 in the quality of life score assessed by the "Venous Insufficiency Epidemiological and Economic Study - Quality of Life / Symptom" (VEINES-QOL / Sym) questionnaire comparing the pre-intervention evaluation and after 90 days of intervention .

Countries

Brazil

Contacts

Public ContactGerli Herr

Universidade Regional do Noroeste do Estado do Rio Grande do Sul - UNIJUI

gerli.herr@unijui.edu.br+5555991636055

Outcome results

None listed

Source: REBEC (via WHO ICTRP) · Data processed: Mar 1, 2026