Effect of Child Delivery on Intraocular Pressure

NCT01174342 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 30

Last updated 2013-01-14

Study results available
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Summary

The purpose of this study is to evaluate the effect of child delivery on the intraocular pressure in healthy women.

Conditions

  • Intraocular Pressure
  • Delivery, Obstetric

Sponsors & Collaborators

  • Meir Medical Center

    lead OTHER

Principal Investigators

  • Fani Segev, M.D. · Meir Medical Center

  • Noa Geffen, M.D. · Meir Medical Center

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-08-31
Primary Completion
2012-08-31
Completion
2012-08-31

Countries

  • Israel

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01174342 on ClinicalTrials.gov