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Ensaios ClĂnicos (somente visualização)
Listagem completa dos ensaios clĂnicos importados do XML ICTRP.
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Id:
9139
Trial ID:
RBR-10tkjh3t
Public Title:
Effectiveness and durability of ready-to-use botulinum toxin A formulations (Relfydess and Alluzience) for treating moderate to severe frown lines: a randomized controlled clinical trial
Scientific Title:
Efficacy and durability of liquid formulations of botulinum toxin type A, Relabotulinumtoxin-A (Relfydess) and RTU Abobotulinumtoxin-A (Alluzience), in the treatment of moderate-to-severe dynamic glabellar lines: a randomized, controlled, triple-blind clinical study
Scientific Title Native:
None
Recruitment Status:
Recruitment completed
Study Type:
Intervention
Study Design:
3, randomized-controlled, triple-blind
Study Phase:
None
Allocation:
None
Masking:
None
Purpose:
None
Date Registration:
2026-04-26
Date Enrolment:
2026-02-01
Last Refreshed:
None
Source Register:
None
Primary Sponsor:
Centro Universitário Uningá
Secondary Sponsors:
None
Web Address:
None
Target Size:
None
Inclusion Criteria:
female patients aged between 25 and 50 years; presence of dynamic glabellar lines involving the procerus and corrugator muscles; no botulinum toxin injections within the last year for aesthetic or therapeutic purposes in any body region; moderate to severe glabellar lines according to the 5-point Merz scale; and no aesthetic procedures performed in the upper third of the face within the last year. 3. Moderate to severe glabellar lines according to the 5-point Merz scale; 4. No other aesthetic procedures performed in the upper third of the face within the last year.
Exclusion Criteria:
receipt of tetanus or COVID-19 vaccination within the last three months prior to study initiation; presence of autoimmune diseases; pregnancy or breastfeeding; presence of neuromuscular disorders, such as myasthenia gravis or Lambert–Eaton syndrome; current use of medications affecting neuromuscular junctions; engagement in high-intensity physical exercise; and refusal or inability to sign the Informed Consent Form
Health Conditions:
None
Interventions Summary:
None
Contacts Summary:
None
Results:
None
Countries:
None
Updated On:
2026-05-11 05:23:18