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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT02154945
Other study ID # 33-2013.CTIL
Secondary ID
Status Withdrawn
Phase N/A
First received May 28, 2014
Last updated January 12, 2016
Start date January 2016
Est. completion date January 2016

Study information

Verified date June 2014
Source The Baruch Padeh Medical Center, Poriya
Contact n/a
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Observational

Clinical Trial Summary

Purpose:

Primary: to prospectively measure Retinal Nerve Fiber Layer (RNFL) and macular thickness changes during pregnancy by Optical coherence tomography

Secondary: The effect of pregnancy abnormalities on RNFL and macular thickness in participants who develop systemic or ocular complications during the study period.


Description:

There are several known ophthalmic physiologic changes in pregnancy:

1. Refractive Change: progesterone-mediated changes in fluid content partially accounts for refractive change of lens and cornea; myopic shift of less than 1 D was observed in in 15% of participating pregnant women

2. Night vision decreased mainly with low serum vitamin A levels in pregnant women.

3. Fall of the IOP in second half of pregnancy (about 10% drop)

4. Corneal changes (increased thickness; decreased sensitivity) = contact lens intolerance

The retina and optic nerve are considered part of central nervous system, the retina and choroid are highly vascularized. Due to changes in CSF and brain volume, vascular and fluid changes all over the pregnant woman's body we expect to find changes in RNFL and macular thickness during pregnancy.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date January 2016
Est. primary completion date January 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria:

- 1st trimester (6-14w) pregnant healthy women

- No known medical problems related to their current pregnancy on recruitment

- Age 18-45yrs

- No known retinal or optic nerve disease

- Refraction between +3.0 and -4.0 diopters

- Agrees to participate in the study

Exclusion Criteria:

- Retinal or optic nerve disease

- Refractive errors more than +3.0 and -4.0.

- If already finished 14w gestation when recruited to the 1st OCT examination

- Known to have HTN or DM before gestation

- Ocular media abnormality that obscures OCT view or examination

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Israel Baruch Padeh Medical Center Poriya Lower Galeli

Sponsors (1)

Lead Sponsor Collaborator
The Baruch Padeh Medical Center, Poriya

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary Retinal nerve fiber layer(RNFL) and Macular thickness by Optical coherence tomography(OCT) during pregnancy The RNFL, measured in micrometers, will be followed up during the study. Every trimester (starting at the 1st trimester) an OCT will be performed measuring the thickness of the RNFL.
An OCT will be performed 3 months postpartum as a control.
The Macular thickness will be measured in the same manner.
1 year Yes
Secondary Effect of systemic and ocular diseases on Retinal Fiber Layer and Macula during pregnancy If systemic or ocular diseases appear during the study, they will be followed up and observed for changes in retinal fiber layer thickness and macular thickness. 1 year Yes
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