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NCT Number: NCT06766799

Comparison Between Handheld Rebound Tonometer and Applanation Tonometer in IOP Measurement in Paediatric Glaucomas

To compare the accuracy between handheld rebound tonometer & applanation tonometer in IOP measurement in pediatric glaucoma cases

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Key information

Age range

3 year–18 year

Sex eligibility

All sexes

Study type

Observational

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients attending to our pediatric glaucoma clinic diagnosed with glaucoma aged >18 years old are subjected to IOP Measurements.

Exclusion criteria

  • **Patients aged more than 18 years old
  • patients with scarred cornea

Treatment and study plan

Rebound and Applanation Tonometer

Device

Measurement of Intraocular Pressure

Primary outcomes

  1. Comparison between the IOP Measurments by Rebound Tonometer & Applanation tonometer

    Time frame: over nine months

    To compare the accuracy between handheld rebound tonometer & applanation tonometer in IOP measurement in pediatric glaucoma cases

Sponsors and collaborators

Lead sponsor

Sohag University

Other

Registry information

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Jan 9, 2025
Registry last updated
Jan 9, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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