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Study of the effect of phenol peeling blephroplasty for the periocular rejuvenation

Evaluation and comparison of side effects and satisfaction of patient and physician in Micropunch Blepharopeeling versus blepharoplasty of the Upper Eyelids for Periorbital Rejuvenation in patients who referred to Alzahra hospital in 2016

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016110330682N1
Enrollment
20
Registered
2016-12-07
Start date
2015-07-23
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

Blepharochalasis. Blepharochalasis

Interventions

Intervention 1: After cleaning the face and injecting the local anesthetic in the upper eyelid region in the blepharopeeling group, peeling is performed in all the periocular region using phenol 89% a
Treatment - Surgery
After injecting the local anesthetic in the blepharoplasty group, the cuts are suprtficially performed with surgery blade NO.15 through the epiderm of the skin which have previously been marked are ta
After cleaning the face and injecting the local anesthetic in the upper eyelid region in the blepharopeeling group, peeling is performed in all the periocular region using phenol 89% and a cotton appl

Sponsors

Deputy of research of Isfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to No maximum

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

MeasureTime 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

MeasureTime 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

Public ContactDr Behzad Bafandeh

Isfahan University of Medical Science

b.bafandeh@resident.mui.ac.irbehzad.bafandeh@gmail.combehzad_bafandeh@yahoo.com+98 31 3668 5555

Outcome results

None listed

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