Blepharochalasis. Blepharochalasis
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Inclusion criteria: age over 40 years; skin type : Fitzpatrick I-III; skin thickness : thin to medium; periorbitally scattered wrinkles; upper eyelid medial or lateral mild- to- medium Ptosis and informed Satisfaction to participate in the study Exclusion criteria: previous local treatment; patients dissatisfaction.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Rate of the patient's satisfaction for eyelid prolapse. Timepoint: two months after operation. Method of measurement: questionnaire.;Rate of the patient's satisfaction for symmetry. Timepoint: two months after operation. Method of measurement: questionnaire.;Rate of the physician's satisfaction with the upper eyelid flaccidity decrease. Timepoint: two months after operation. Method of measurement: observation.;Rate of the patient's satisfaction for esthetics. Timepoint: two months after operation. Method of measurement: questionnaire.;Rate of the patient's general satisfaction. Timepoint: two months after operation. Method of measurement: questionnaire. | — |
Secondary
| Measure | Time frame |
|---|---|
| Periorbital erythema. Timepoint: daily up to one week and then 2 weeks and 2 months after treatment start. Method of measurement: Visit, history and physical examination.;Hypopigmentation. Timepoint: daily up to one week and then 2 weeks and 2 months after treatment start. Method of measurement: Visit, history and physical examination.;Hyperpigmentation. Timepoint: daily up to one week and then 2 weeks and 2 months after treatment start. Method of measurement: Visit, history and physical examination.;Scar. Timepoint: daily up to one week and then 2 weeks and 2 months after treatment start. Method of measurement: Visit, history and physical examination.;Hematoma. Timepoint: daily up to one week and then 2 weeks and 2 months after treatment start. Method of measurement: Visit, history and physical examination.;Granuloma. Timepoint: daily up to one week and then 2 weeks and 2 months after treatment start. Method of measurement: Visit, history and physical examination.;Infection. Timepoint: daily up to one week and then 2 weeks and 2 months after treatment start. Method of measurement: Visit, history and physical examination.;Dry eye syndrome. Timepoint: daily up to one week and then 2 weeks and 2 months after treatment start. Method of measurement: Visit, history and physical examination.;Edema. Timepoint: daily up to one week and then 2 weeks and 2 months after treatment start. Method of measurement: Visit, history and physical examination.;Bruising. Timepoint: daily up to one week and then 2 weeks and 2 months after treatment start. Method of measurement: Visit, history and physical examination.;Loss of vision. Timepoint: daily up to one week and then 2 weeks and 2 months after treatment start. Method of measurement: Visit, history and physical examination.;Diplopia. Timepoint: daily up to one week and then 2 weeks and 2 months after treatment start. Method of measurement: Visit, history and physical examination.;Lagophtalmos. Timepoint: daily up to one w | — |
Countries
Iran (Islamic Republic of)
Contacts
Isfahan University of Medical Science