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Corneal Biomechanics During Pregnancy

Change in Corneal Biomechanics During Pregnancy

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04433689
Acronym
CorvisPreg
Enrollment
50
Registered
2020-06-16
Start date
2016-01-01
Completion date
2021-01-31
Last updated
2020-06-22

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

Conditions

Pregnancy

Keywords

pregnancy, corneal biomechanical properties, intraocular pressure

Brief summary

It is known that intraocular pressure changes during pregnancy. Collagen structure changes during pregnancy to enable softening of the symphysis, whitening of the birth chanel, and, thus, ultimately to enable delivery of a child. The cornea consists of highly structured collagen fibers. Hence, it seams logically that corneal biomechanics also change during pregnancy.

Detailed description

It is known that intraocular pressure changes during pregnancy. Collagen structure changes during pregnancy to enable softening of the symphysis, whitening of the birth chanel, and, thus, ultimately to enable delivery of a child. The cornea consists of highly structured collagen fibers. Hence, it seams logically that corneal biomechanics also change during pregnancy. Measurement of intraocular pressure is highly dependant on corneal properties. With the Corvis ST device by Ocular Inc. it is possible to measure intraocular pressure and investigated corneal biomechanics. The aim of this study is therefore to compare corneal biomechanical properties during the third trimester with corneal biomechanical properties at 3 months after delivery.

Interventions

DEVICENon-Contact measurement of corneal properties

Corneal Properties will be measurement with the non-contact Corvis ST Air-Puff Tonometer by Oculus Inc.

Sponsors

University of Zurich
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 38 Years
Healthy volunteers
Yes

Inclusion criteria

* females * pregnant * age 18 to 38 yo * uncomplicated singleton pregnancy

Exclusion criteria

* any history of ocular disease or surgery other than conjunctivitis, especially no history of glaucoma or corneal disease * systemic diseases, i.e. diabetes, hypertension, collagenase * current contact lens wear * before pregnancy taking any systemic or ocular medications

Design outcomes

Primary

MeasureTime frameDescription
Change in Deformation Amplitudeat 3 month post delivery compared to during third trimesterChange in Deformation Amplitude (in millimeters) at 3 month post delivery compared to during third trimester will be assessed.
Change in Applanation Lengthat 3 month post delivery compared to during third trimester of the pregnancyChange in Applanation Length (in millimeters) at 3 month post delivery compared to during third trimester of the pregnancy will be assessed.
Change in Corneal Velocityat 3 month post delivery compared to during third trimester of the pregnancyChange in Corneal Velocity (in meters/second) at 3 month post delivery compared to during third trimester of the pregnancy will be assessed.
Change in corneal thicknessat 3 month post delivery compared to during third trimester of the pregnancyChange in corneal thickness (in millimeters) at 3 month post delivery compared to during third trimester of the pregnancy will be assessed.
Change in Intraocular pressureat 3 month post delivery compared to during third trimester of the pregnancyChange in intraocular pressure (in millimeters of mercury, mmHg) at 3 month post delivery compared to during third trimester of the pregnancy will be assessed.

Countries

Switzerland

Contacts

Primary ContactMarc o Toeteberg-Harms, MD, FEBO
marc.toeteberg@usz.ch+41442551111
Backup ContactBelgin o Özsoy, MD
belgin.oezsoy@usz.ch+41442551111

Outcome results

None listed

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