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Evaluation of the Outcomes of Endoscopic Facelift and Forehead Lift Surgery Under Local Anesthesia in Patients Referred to the Clinic in 2025.

Evaluation of the Outcomes of Endoscopic Facelift and Forehead Lift Surgery Under Local Anesthesia in Patients Referred to the Clinic in 2025.

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20231030059908N6
Enrollment
25
Registered
2025-10-22
Start date
2025-09-23
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

A new method of cosmetic surgery.. Encounter for cosmetic surgery

Interventions

Intervention group: 25 eligible patients will be selected for the study and after obtaining written consent, their demographic information and medical history will be reviewed and recorded in the data

Sponsors

Islamic Azad University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 45 Years

Inclusion criteria

Inclusion criteria: Patients who are candidates for endoscopic forehead and face lift surgery. Age range 30 to 45 years. having very thick skin on the forehead. Patient consent to participate in the study.

Exclusion criteria

Exclusion criteria: Smoking Having an underlying disease such as high blood pressure, diabetes, etc. Having severe wrinkles on the forehead. Having very thick skin on the forehead. Trauma to the forehead and face.

Design outcomes

Primary

MeasureTime frame
Clinical results of surgery. Timepoint: Before the intervention and 6 months after surgery. Method of measurement: Ruler.;Degree of improvement in facial and forehead wrinkles. Timepoint: Before the intervention and 6 months after surgery. Method of measurement: The opinion of the doctor and the patient themselves.;Incidence of side effects (infection, bleeding, nerve damage, etc.). Timepoint: Before the intervention and 6 months after surgery. Method of measurement: The opinion of the doctor and the patient themselves.;Degree of patient satisfaction with surgical results. Timepoint: Before the intervention and 6 months after surgery. Method of measurement: Baker scale.;Recovery time (days elapsed until return to normal activities). Timepoint: At the beginning of the intervention, 14 and 21 days after the completion of surgery. Method of measurement: The opinion of the doctor and the patient themselves.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAmir Asdaleh Khajeh Rahimi

Islamic Azad University

aa.khajerahimi@yahoo.com+98 21 3334 8036

Outcome results

None listed

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