Surgical Procedure, Unspecified Clinical Trial
Official title:
Lateral Rectus Muscle Tendon Elongation by an Auto Graft From the Resected Medial Rectus Muscle as a Monocular Surgery for Large Angle Sensory Exotropia
NCT number | NCT04286945 |
Other study ID # | 21423 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | January 1, 2017 |
Est. completion date | September 1, 2018 |
Verified date | February 2020 |
Source | Tanta University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
To evaluate a technique using resected medial rectus muscle transplantation for elongation of Lateral rectus tendon as a monocular surgery for large angle sensory exotropia.
Status | Completed |
Enrollment | 16 |
Est. completion date | September 1, 2018 |
Est. primary completion date | June 1, 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 7 Years and older |
Eligibility |
Inclusion Criteria: - Patients with monocular low vision or loss of vision due to congenital or acquired cause with exodeviation of the poorly seeing eye = 50PD. Exclusion Criteria: - Patients with exotropia other than sensory type (alternating exotropia, intermittent exotropia) - Angle of deviation less than 50 PD. - visual acuity more than 0.2 decimal in affected eye . - A or V pattern exotropia. - Nystagmus . - Refusal of surgery by the adult patients or caregiver of children. |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Tanta University |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Distant angle of deviation after surgical correction | Measured by alternate prism cover test for near and far,which is considered successful if within10 prism diopter esotropia or exotropia. | 6month | |
Primary | limitation of adduction and abduction | measured by a scale from -4 to 0; with-4 implying no adduction or abduction beyond midline, -3 implying for 75% deficit,-2 for 50% deficit,-1 for 25% deficit and 0 for full ductions. | 6month | |
Primary | patient satisfaction with the procedure | score assesed by questionnaire of 3questions based on satisfaction with degree of alignment, aesthetic appearance, limitation of adduction and abduction. 0: I am not satisfied, 1: I am moderately satisfied, 2: I am satisfied, 3: I am very satisfied, and Iwould recommend it to another. Based on the score (0-3 unsatisfied, 4-6 moderately satisfied, 7-9 very satisfied). |
after 6 month |
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