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New Surgical Approach in Labioplasty

New Surgical Approach in Labioplasty: Inspired by the Fibonacci Ratio

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05988151
Enrollment
100
Registered
2023-08-14
Start date
2022-04-12
Completion date
2023-08-02
Last updated
2023-10-17

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

Conditions

Gynecologic Disease, Surgery-Complications

Keywords

Labioplasty, Vaginoplasty, Fibonacci ratio

Brief summary

The data of patients who underwent labiaplasty + vaginoplasty between 2020 and 2022 by a single surgeon in our clinic were analyzed. Preoperative and postoperative FSFI (Female sexual function index) questionnaire scores were used to compare the results of the classical surgical approach and the new surgical approach technique designed according to the Fibonacci ratio in the early postoperative period such as operating time, bleeding amount, etc.

Detailed description

The data of patients who underwent labiaplasty + vaginoplasty between 2020-2022 for reasons such as vaginal laxity, personal hygiene problems, recurrent vaginal infections were analyzed retrospectively. The data of the patients who underwent fibonacci ratio, which is a new surgical approach technique( by Okuyan E. M.D), and the patients who underwent classical surgical technique were taken from their files and retrospectively analyzed. Data including age, body mass index, number of live births, preoperative FSFI, FGSIS and postoperative one month FSFI (Female sexual function index) and FGSIS (The Female Genital Self-Image Scale) scores were recorded and compared between both groups.

Interventions

OTHERNew surgical approach

Patients were included in the study after obtaining informed consent for the new surgical approach inspired by the Fibonacci ratio.

Sponsors

Batman Training and Research Hospital
Lead SponsorOTHER_GOV

Study design

Observational model
CASE_CONTROL
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

1. No history of any disease 2. The presence of at least 2 of the reasons such as dislike of cosmetic appearance, vaginal abundance, personal hygiene disorder, difficulty in wearing underwear. 3. Body mass index between 15-25 4. Informed consent has been obtained for the new surgical approach technique. 5. Not taking any medication continuously 6. Willing to participate in the study.

Exclusion criteria

1. Absence of at least 2 of the reasons such as dislike of cosmetic appearance, vaginal abundance, personal hygiene disorder, difficulty in wearing underwear. 2. History of continuous medication, alcohol and/or smoking. 3. History of chronic diseases (Asthma, Diabetes mellitus, Cardiac disease, Psychiatric disease etc.) 4. Body mass index outside the range of 15-25. 5. Not wanting to be included in the study or wanting to leave the study after inclusion.

Design outcomes

Primary

MeasureTime frameDescription
To be able to standardize genital harmony using fibonacci ratio.Postoperative 1 monthTo standardize the genital harmony with a holistic approach with the Fibonacci ratio with a purely mathematical ratio outside the existing classification systems (in contrast to Banwell, Motakeff classifications).

Secondary

MeasureTime frameDescription
To adapt the fibonacci ratio to female genital cosmetic surgeryPostoperative 1 monthTo adapt the fibonacci ratio applied in breast and facial aesthetics to female genital aesthetic surgery procedures.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026