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Tests to prove the efficacy and safety of Bandage Active Gueds in humans affected by vascular wound

Single-blind clinical study on the efficacy and safety of the Gueds Active Bandage

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-92y48wx
Enrollment
Unknown
Registered
2025-01-24
Start date
2024-10-31
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

Interventions

To prove the efficacy and safety of the Gueds Active Bandage in humans with vascular wounds and demonstrate the product's effect on faster skin regeneration for damaged or injured tissue. This is a ra

Sponsors

Instituto de Saúde e Bem Estar da Mulher
Lead Sponsor
Nipo Serviços Médicos SS Ltda
Collaborator

Eligibility

Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Participating patient who has Venous Vascular Ulcers and/or Lymphatic Edema. Whit woounds that require bandages and compression bandages. Age between 18 and 80 years. Any ethinicity, color/race, phototypes. Both sexes

Exclusion criteria

Exclusion criteria: Pregnancy. Neonates (0 to 1 year old). Sensitivity to the components of the medicine. Patients with ulcers caused by diabetes mellitus, arterial ulcers and mixed ulcers. Carrier of weakened limbs

Design outcomes

Primary

MeasureTime frame
Demonstrate the efficacy of Gueds Active Bandage in humans

Secondary

MeasureTime frame
No secondary outcomes are expected

Countries

Brazil

Contacts

Public ContactFrederico Viana

TCI Laboratório Biotecnológico Ltda

frederico@tcilab.com.br+55 38 99886-3565

Outcome results

None listed

Source: REBEC (via WHO ICTRP)