Comparison of CO2 Laser Assisted Upper Lid Blepharoplasty by Two Different Methods

Comparison of Clinical Outcomes of CO2 Laser Assisted Upper Lid Blepharoplasty by Two Different Methods: a Randomized Clinical Trial Study

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20180302038917N1

Enrollment

Registered

2018-11-13

Start date

2018-09-23

Completion date

Unknown

Last updated

2019-01-14

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

Conditions

Bilateral Mild to Sever Ptosis of Upper lids. Ptosis of eyelid

Interventions

Intervention 1: Intervention group 1: On One Side is used for cutting the Skin. Other Surgical Procedures will be Laser-based. Intervention 2: Intervention group 2: On the other Side the CO2 Laser is

Eligibility

Sex/Gender

All

Age

20 Years to 60 Years

Inclusion criteria

Inclusion criteria: Normal Ophtalmic Examination Bilateral Mild to Sever Ptosis of Upper Lids

Exclusion criteria

Exclusion criteria: Anticoagulant Therapy Coagulopathy Disorders Causing Peripheral Neuropathy such as Diabetes Mellitus History of Trauma or Surgery of Upper Lids Skin Disorders

Design outcomes

Primary

Measure	Time frame
Scar at the field of surgery. Timepoint: after 60 days. Method of measurement: Manchester scar scale.;Edema. Timepoint: days of 1, 3, 7, 14 and 30 after surgery. Method of measurement: Likert scale.;Ecchymosis. Timepoint: days of 1, 3, 7, 14 and 30 after surgery. Method of measurement: Likert scale.;Erythema. Timepoint: days of 1, 3, 7, 14 and 30 after surgery. Method of measurement: Likert scale.	—

Measure

Time frame

Scar at the field of surgery. Timepoint: after 60 days. Method of measurement: Manchester scar scale.;Edema. Timepoint: days of 1, 3, 7, 14 and 30 after surgery. Method of measurement: Likert scale.;Ecchymosis. Timepoint: days of 1, 3, 7, 14 and 30 after surgery. Method of measurement: Likert scale.;Erythema. Timepoint: days of 1, 3, 7, 14 and 30 after surgery. Method of measurement: Likert scale.

—

Secondary

Measure	Time frame
Patients satifaction. Timepoint: after 60 days. Method of measurement: Likert Scale.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMilad Alikazemi

Ahvaz University of Medical Sciences

alikazemi.m@ajums.ac.ir+98 61 3322 2818

Outcome results

None listed

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