Actively Recruiting

Phase 2
Age: 18Years +
All Genders
Healthy Volunteers
NCT06465056

Use of Botulinum Toxin A in Direct Eyebrow Lift Scar

Led by University of Sao Paulo · Updated on 2024-06-18

40

Participants Needed

2

Research Sites

104 weeks

Total Duration

On this page

Sponsors

U

University of Sao Paulo

Lead Sponsor

U

University of Campinas, Brazil

Collaborating Sponsor

AI-Summary

What this Trial Is About

Prospective, controlled and randomized study in which participants indicated for surgery to direct eyebrow lift will be randomized into two groups. In addition to surgery, the patients will be treated with botulinum toxin in one eyebrow and saline (placebo) in the other site. The patients participate as treatment and placebo at the same time. Assessments will be carried out through non-invasive exams.

CONDITIONS

Official Title

Use of Botulinum Toxin A in Direct Eyebrow Lift Scar

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients over 18 years of age with indication for direct eyebrow lift surgery.
Not Eligible

You will not qualify if you...

  • Vulnerable groups: children, pregnant women and immunosuppressed patients
  • Allergy to botulinum toxin A
  • Patients under 18 years old
  • Women who are breastfeeding
  • Patients with muscular/neuromuscular diseases such as myasthenia gravis and amyotrophic lateral sclerosis
  • Patients who underwent botulinum toxin A injection in the last 6 months prior to surgery
  • Patients with a history of radiotherapy, chemotherapy or hematological disorders
  • Refusal to participate in the study

AI-Screening

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Trial Site Locations

Total: 2 locations

1

University of São Paulo (Clinical Hospital)

São Paulo, Brazil, 05403-010

Actively Recruiting

2

Ophthalmology Dept. University of Sao Paulo General Hospital

São Paulo, Brazil, 05403010

Actively Recruiting

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Research Team

R

Renata Lemos

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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