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Dysport in the treatment of forehead & glabellar lines

Evaluation of efficacy and side effects of dysport in the treatment of forehead & glabellar lines in individuals with forehead & and glabellar lines

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201209179844N2
Enrollment
60
Registered
2012-09-23
Start date
2012-04-05
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

forehead & glabellar lines. Other disorders of skin and subcutaneous tissue, not elsewhere classified

Interventions

For all individuals botulinum toxin (Dysport) in 2 ml saline normal for subdermal injection according to the Dysport company protocol will be administered..
Treatment - Drugs
For all individuals botulinum toxin (Dysport) in 2 ml saline normal for subdermal injection according to the Dysport company protocol will be administered.

Sponsors

Vice chancellor for research, Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: (to be 18 to 55 years old; not to be pregnant) Exclusion criteria: (to perform other cosmetic procedures during the study; presence of visible scar; prior cosmetic procedures which might interfere with Dysport response; significant facial asymetria; ptosis; dermatochalasis; failure in reduction of glabellar lines even with physical traction; neurologic disorders such as myasthenia gravis; ALS and neuromascular disorders or history of facial weakness; infection of injection site; use of aminoglycosides of any kind)

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Response to the treatment. Timepoint: 2, 8, 12, 16, 20, 24 weeks after the treatment. Method of measurement: Physical examination and taking pictures from the lines.

Secondary

MeasureTime frame
Side effects. Timepoint: 2, 4, 8, 12, 16, 20, 24 weeks after the treatment. Method of measurement: Physical examination and history.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMorteza Mohammadi

Tabriz University of Medical Sciences

morteza_mohammadi2010@yahoo.com+98 41 1658 4305

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026