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OpenTrials
Completed

NCT Number: NCT01435876

Surgery and Convergence Insufficiency Intermittent Exotropia

This trial aims to determine which treatment modality is better for treatment of the convergence insufficiency subtype of intermittent exotropia.

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Key information

Conditions

Complications

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Aditya Sudhalkar, Ahmedabad, Gujarat, India

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About this study

Surgery can give better results,

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

Convergence Insufficiency Type Intermittent Exotropia

  • No stereopsis
  • Good visual acuity

Exclusion criteria

  • Amblyopia
  • Anisometropia > 2.5D
  • Vertical deviations

Treatment and study plan

Post exercise Surgery

Procedure

ORTHOPTICS/MINUS LENS THERAPY

Other names: Accomodative therapy

Orthoptics

Procedure

MINUS LENS THERAPY/ ORTHOPTICS

Other names: MINUS LENS THERAPY/ORTHOPTICS

Postop orthoptics

Procedure

ORTHOPTICS/MINUS LENS THERAPY

Other names: Minus Lens Therapy

Post exercises surgery

Procedure

UNIOCULAR/BINOCULAR RECESSION/RESECTION

Other names: Minus Lens Therapy

Primary outcomes

  1. Postoperative gain of stereopsis

    Time frame: 1month-1 year

Sponsors and collaborators

Lead sponsor

Sudhalkar Eye Hospital

Other

Registry information

Official study title

Treatment for Convergence Insufficiency Intermittent Exotropia; A Randomized Trial

Important dates

Study start
2006
Primary completion
2010
Study completion
2011
First posted
Sep 19, 2011
Registry last updated
Sep 19, 2011

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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