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CompletedNCT07693673Updated Jul 9, 2026

Corneal Topography and High Order Aberrations in Regular Contraceptive Pills

An observational study in Cornea and Refraction Error, sponsored by Elshimaa A.Mateen. Completed at 1 site in Egypt. Open to female participants aged 18 Years to 40 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-07-09.

Sponsored by Elshimaa A.Mateen · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
40
Ages
18 Years to 40 Years
Sex
Female
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Study summary

Effect of regular usage of contraceptive pills on corneal topography and corneal high-order aberrations

Read the detailed description

Comparing corneal topographic changes and corneal high-order aberrations for women planning to use oral contaceptive pills before and after the usage of the pills

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Conditions studied

  • Cornea
  • Refraction Error

Keywords

  • cornea-contraceptive pills-high order aberrations
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In context

Corneal Diseases

130 studies on the registry are indexed under Corneal Diseases; 43 are open to participants now.

This study's enrollment of 40 is below the median of 102 across 46 observational studies indexed under Corneal Diseases.

Browse Corneal Diseases studies →

Lead sponsor

Elshimaa A.Mateen is the lead sponsor of 2 studies on the registry; 1 is open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 40 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Premenopausal women aged 18-40 years attending the Ophthalmology Department at Sohag University Hospital who are prescribed combined oral contraceptive pills by their gynecologist as part of routine clinical care. Participants will undergo corneal topography and tomography before starting treatment and after 1 year of oral contraceptive use.

Inclusion criteria

  • Female participants aged 18-40 years.
  • Prescribed combined oral contraceptive pills as part of routine gynecological care.
  • Willing to undergo corneal topography/tomography before starting treatment and after 1 year.
  • No previous history of corneal disease or ocular surgery.
  • Able to provide informed consent.

Exclusion criteria

Exclusion Criteria:

  • Keratoconus or suspected corneal ectasia.
  • Corneal opacity, dystrophy, degeneration, or scarring.
  • Previous ocular surgery or significant ocular trauma.
  • Current contact lens use or recent contact lens use without adequate discontinuation period.
  • Active ocular surface disease or severe dry eye.
  • Glaucoma, uveitis, retinal disease, or other significant ocular pathology.
  • Diabetes mellitus, autoimmune disease, thyroid disease, pregnancy, or lactation.
  • Use of other hormonal therapy or systemic medications known to affect corneal parameters.
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
40 participants (actual)
Patient registry
No

Groups and cohorts

  • Oral contraceptive pills users

    Other: Hormonal Contraception · Drug: Combined Oral Contraceptive (COC)

Interventions

  • OtherHormonal Contraception

    Effect of usage of hormonal contraceptive pills on corneal topography and corneal high-order aberrations

  • DrugCombined Oral Contraceptive (COC)

    Participants who are prescribed combined oral contraceptive pills as part of routine clinical care will be observed. Corneal topography and tomography will be performed before starting treatment and after the follow-up period to evaluate changes in corneal parameters.

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What researchers measure

Primary outcomes

  1. Change in K1 (D)

    Time frame: Baseline and 1 year

  2. Change in K2 (D)

    Time frame: one year

  3. Change in Kmax (D)

    Time frame: one year

  4. change in corneal thickness (um)

    Time frame: one year

07

Study locations

1 site
  • Ophthalmology Department, Sohag University Hospital, Faculty of Medicine, Sohag University
    Sohag, Sohag Governorate 82524, Egypt
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 9, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07693673
Lead sponsor
Elshimaa A.Mateen
Responsible party
Elshimaa A.Mateen (Assistant Professor, Sohag University) — Sponsor-investigator
First posted
Jul 9, 2026
Start date
Oct 1, 2024
Primary completion
Jan 30, 2026
Completion
Mar 30, 2026
Last update
Jul 9, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jun 2026. You cannot join it, but the record below documents what was studied.

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