N/A
N=30
Effect of Child Delivery on Intraocular Pressure
Intraocular Pressure · Delivery, Obstetric
Bottom Line
View on ClinicalTrials.gov: NCT01174342 ↗Enrolled (actual)
30
Serious AEs
0.0%
Results posted
Dec 2012
Primary outcome: Primary: Intraocular Pressure — 11.8; 11.9; 11.8; 12.1 mm Hg
Study Design & Population
- Study type
- Observational
- Phase
- N/A
- Interventions
- —
- Age
- Adult · 18+ yrs
- Sex
- Female
- Sponsor
- Meir Medical Center
- Primary completion
- Aug 2012
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Intraocular Pressure |
11.8; 11.9; 11.8; 12.1; 12.2; 11.9 | — |
Summary
The purpose of this study is to evaluate the effect of child delivery on the intraocular pressure in healthy women.
Eligibility Criteria
Inclusion Criteria
- Age ≥ 18 years.
- Pregnant women admitted to the labor room.
- Healthy women that do not take any systemic medications.
- No known ocular condition, except for refraction errors, strabismus or amblyopia.
- Eligible women who are able to sign an informed consent form.
Exclusion Criteria
- Family history of glaucoma (first degree relatives).
- Known allergic reaction to local anesthesia (oxybuprocaine hydrochloride).
- Women who are unable to sign an informed consent form.
Data sourced from ClinicalTrials.gov (NCT01174342). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.