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Esotropia clinical trials

View clinical trials related to Esotropia.

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NCT ID: NCT02413463 Completed - Clinical trials for Partially Accommodative Esotropia

Augmented Medial Rectus Muscle Recession Versus Posterior Scleral Fixation in Partially Accommodative Esotropia

Start date: January 2015
Phase: N/A
Study type: Interventional

Prospective randomized interventional comparative study

NCT ID: NCT02404324 Active, not recruiting - Esotropia Clinical Trials

Conservative Treatment of Esotropia in Children up to 3 Years Old

Start date: January 2012
Phase: N/A
Study type: Interventional

The objective of this prospective study is the treatment of esotropia by prescribing the full precise optical correction of refractive errors in children up to 3 years old.

NCT ID: NCT01616108 Recruiting - Strabismus Clinical Trials

Bupivacaine Injection of Eye Muscles to Treat Strabismus

Start date: April 2012
Phase: Phase 2/Phase 3
Study type: Interventional

This study seeks to determine if bupivacaine injection of eye muscles can make them stronger and stiffer, and thereby correct the position of eyes that are turned in or mis-aligned, a condition generally termed strabismus. It seeks further to find out the different effects of various concentrations or formulations of bupivacaine, and whether addition of Botox to other eye muscles can add to the effect of bupivacaine and enhance the correction of strabismus.

NCT ID: NCT01460355 Completed - Exotropia Clinical Trials

Comparison of Two Treatments for Strabismus Correction: Botulinum Toxin A Associated to Surgery and Surgery Alone

Start date: September 2006
Phase: Phase 4
Study type: Interventional

Two different treatments were given to large angle horizontal strabismus (eso and exotropia) adult patients who agree to participate of the study. Inform consents were required for participants. Group 1 (12 patients) received conventional recess-resect surgery plus intraoperative injection of botulinum toxin A (5U). Group 2 (11 patients) received only conventional recess-resect surgery. The patients were randomly located in one of the groups. The angles of horizontal deviation were compared between the groups before and six months after treatment.

NCT ID: NCT01179711 Completed - Clinical trials for Accommodative Esotropia

Under-correction in Refractive Accommodative Esotropia

Start date: June 2009
Phase: N/A
Study type: Interventional

In most clinics, physicians reduce diopter of hyperopic glasses in older patients with accommodative esotropia. However, there are risks of decompensation in that practice. The authors are going to try measure the change of stability of eye alignment after reducing diopter of hyperopic glasses.

NCT ID: NCT01166503 Completed - Esotropia Clinical Trials

Early Versus Delayed Surgery for Infantile Esotropia

Start date: May 2004
Phase:
Study type: Observational

The goal of this study is to determine whether corrective surgery done earlier than the current standard can better improve the visual and eye movement deficits in children with infantile esotropia (crossed eyes in infancy).

NCT ID: NCT00993174 Active, not recruiting - Esotropia Clinical Trials

Surgery for Esotropia Under Topical Anesthesia

SETTA
Start date: May 2004
Phase: N/A
Study type: Interventional

Adult patients requiring surgery for esotropia will be randomized to surgery under topical anesthesia or sub-Tenon's anesthesia. Amount of surgery required with the two anesthetic procedures will be compared. Motor and sensory outcome of the two treatment groups will also be compared.

NCT ID: NCT00746304 Completed - Esotropia Clinical Trials

Long-Term Outcomes in the Treatment of Infantile and Acquired Esotropia With Botulinum Toxin

Start date: September 2007
Phase: N/A
Study type: Observational

To investigate long-term treatment outcomes of patients receiving botulinum toxin A therapy for infantile and acquired esotropia.

NCT ID: NCT00310960 Completed - Infantile Esotropia Clinical Trials

An Observational Study of Infantile, Acquired Non-accommodative, and Acquired Partially-accommodative Esotropia

Start date: June 2004
Phase: Phase 3
Study type: Observational

The purpose of this study is to: - To estimate the duration of misalignment by age at presentation in infantile esotropia (infantile ET), acquired non-accommodative esotropia (ANAET) and acquired partially accommodative esotropia (APAET). - To determine the proportion of patients with angle instability in infantile ET, ANAET and APAET by length of follow-up.

NCT ID: NCT00304577 Completed - Strabismus Clinical Trials

Bilateral Recession or Unilateral Recession-Resection as Surgery for Infantile Esotropia

Start date: January 1998
Phase: Phase 3
Study type: Observational

Infantile esotropia is corrected in most cases by bilateral recession of the medial rectus muscles (BR) or by unilateral recession of the medial rectus muscle and resection of the lateral rectus muscle (RR). We compared the outcome of these techniques in a randomized prospective study.