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Recruiting

NCT Number: NCT07456488

The Effect of 0.01% Atropine Eye Drops on Axial Length and Refraction in Myopic Children Compared to a Control Group

In this study, atropine 0.01% eye drops will be given to myopic children once at night daily for 6 months as compared to a control group to see the effect on axial length and refraction

Recruiting

Interested in participating?

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Key information

Age range

4 year–16 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Children aged 4-16 years
  • Both genders
  • Myopia of baseline SER of -1.00D or more
  • Astigmatism less than or equal to -2.50D
  • No medical history predisposing severe myopia (e.g., Marfan syndrome, Stickler syndrome, and retinopathy of prematurity), abnormal ocular refractive anatomy (e.g., keratoconus, lenticonus, and spherophakia)
  • No history of other vision-threatening ocular diseases or previous intraocular surgery.
  • No current or previous use of atropine or pirenzipine, contact lenses or other forms of treatment that may affect myopia progression.

Exclusion criteria

  • Astigmatism ≥ 2.5 D
  • Anisometropia>1 D
  • Best corrected visual acuity < 0.5 (6/12)
  • Prior intraocular surgery
  • Allergy to atropine eye drops
  • Systemic diseases associated with myopia such as Marfan syndrome, Stickler syndrome
  • History of cardiac or significant respiratory diseases
  • Lack of consent for participating in the study

Treatment and study plan

Atropine 0.01% eye drops

Drug

Eye drops atropine 0.01% given once nightly to group A for 6 months

Primary outcomes

  1. Change in axial length in mm

    Time frame: 6 months

    Axial length is measured at the time of recruiting the participants and after the end of study

  2. Change in refraction in Diopters

    Time frame: 6 months

    Refraction is measured at the start of study then after 6 months of study

Study contacts

Contact information is provided by the study sponsor or research team.

Hina Nadeem, MBBS

CONTACT

[email protected]

03252120568

Sponsors and collaborators

Lead sponsor

Liaquat National Hospital & Medical College

Other

Registry information

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Mar 6, 2026
Registry last updated
Mar 6, 2026

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.