comparison between masport and dysport in facial botox

Comparison of the effects and side effects of Dysport and Masport in patients referred to the ultra-specialized oculoplasty clinic of Farabi Hospital in 1402

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20230727058942N1

Enrollment

160

Registered

2023-12-18

Start date

2023-08-27

Completion date

Unknown

Last updated

2024-01-22

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

Conditions

Investigating the therapeutic effects of two drugs, MASPORT and DYSPORT, on wrinkles around the eyes. forehead. ????? ???????? ???? ??? ? ??? ??

Interventions

Intervention 1: Intervention group: Intervention group 1: under MASPORT injection. Each person is injected with 110 units of medicine that contains the chemical composition of botulinum toxin and is m

Eligibility

Sex/Gender

All

Age

27 Years to 57 Years

Inclusion criteria

Inclusion criteria: Physical and mental health The ability to make decisions regarding voluntary participation in the study Permissible age range in study (27-54 years old) Botox injection candidate in the studied areas

Exclusion criteria

Exclusion criteria: History of heavy surgeries and any type of fracture in any part of the face History of stroke and facial paralysis

Design outcomes

Primary

Measure	Time frame
1- To investigate the effect of two drugs in the same doses in removing and reducing the depth of wrinkles in patients. Timepoint: At the beginning of the study, the day of injection, 14 days later, 2 months later and 4 months after injection. Method of measurement: A questionnaire prepared and completed by the doctor and the patient and photos taken of the target areas before and after the injection, which examines the function of the frown muscles and forehead muscles.;2- Examining the short-acting and long-acting side effects of both drugs, including inflammation, redness, and drooping of the eyelids. Timepoint: At the beginning of the study, the day of injection, 14 days later, 2 months later and 4 months after injection. Method of measurement: A questionnaire prepared and completed by the doctor and the patient and photos taken of the target areas before and after the injection, which examines the function of the frown muscles and forehead muscles.;3- Checking the shelf life of two drugs. Timepoint: At the beginning of the study, the day of injection, 14 days later, 2 months later and 4 months after injection. Method of measurement: A questionnaire prepared and completed by the doctor and the patient and photos taken of the target areas before and after the injection, which examines the function of the frown muscles and forehead muscles.;4- Checking the need for re-injection and restoration of two drugs at intervals of 2 weeks, 2 months and 4 months. Timepoint: At the beginning of the study, the day of injection, 14 days later, 2 months later and 4 months after injection. Method of measurement: A questionnaire prepared and completed by the doctor and the patient and photos taken of the target areas before and after the injection, which examines the function of the frown muscles and forehead muscles.	—

Measure

Time frame

1- To investigate the effect of two drugs in the same doses in removing and reducing the depth of wrinkles in patients. Timepoint: At the beginning of the study, the day of injection, 14 days later, 2 months later and 4 months after injection. Method of measurement: A questionnaire prepared and completed by the doctor and the patient and photos taken of the target areas before and after the injection, which examines the function of the frown muscles and forehead muscles.;2- Examining the short-acting and long-acting side effects of both drugs, including inflammation, redness, and drooping of the eyelids. Timepoint: At the beginning of the study, the day of injection, 14 days later, 2 months later and 4 months after injection. Method of measurement: A questionnaire prepared and completed by the doctor and the patient and photos taken of the target areas before and after the injection, which examines the function of the frown muscles and forehead muscles.;3- Checking the shelf life of two drugs. Timepoint: At the beginning of the study, the day of injection, 14 days later, 2 months later and 4 months after injection. Method of measurement: A questionnaire prepared and completed by the doctor and the patient and photos taken of the target areas before and after the injection, which examines the function of the frown muscles and forehead muscles.;4- Checking the need for re-injection and restoration of two drugs at intervals of 2 weeks, 2 months and 4 months. Timepoint: At the beginning of the study, the day of injection, 14 days later, 2 months later and 4 months after injection. Method of measurement: A questionnaire prepared and completed by the doctor and the patient and photos taken of the target areas before and after the injection, which examines the function of the frown muscles and forehead muscles.

—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactGhazal ghochani

Tehran University of Medical Sciences

Gghochani@gmail.com+98 21 5540 0003

Outcome results

None listed

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