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NCT05425589 Clinical Trial

Adjustable Strabismus Surgery

Strabismus Clinical Trial

Official title:
Adjustable Strabismus Surgery

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT05425589
Other study ID # FUI/CTR/2022/2
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date October 1, 2017
Est. completion date October 1, 2024

Study information
Verified date June 2022
Source Foundation University Islamabad
Contact Sana Nadeem, MBBS, FCPS, ACMEd
Phone +92515788162
Email sana.nadeem@fui.edu.pk
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Strabismus, whether congenital or acquired, is a common visual and cosmetic problem, especially for the young. Adjustable suture strabismus surgery is not in vogue in our country. This technique gives the surgeon a second attempt to provide a better outcome for the patients.

Recruitment information / eligibility
Status Recruiting
Enrollment 50
Est. completion date October 1, 2024
Est. primary completion date January 1, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 5 Years to 69 Years
Eligibility Horizontal, vertical and complex strabismus cases (sensory, paralytic, nystagmus, monocular elevation deficit and dissociated vertical/horizontal deviation) were included, along with patients with a previous history of strabismus surgery. Myasthenia gravis was excluded along with noncooperative children; less than 7 years of age. Those who did not return for a one year follow up also had to be excluded.

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Adjustable strabismus surgery
Our objective was to assess the long-term success of adjustable suture strabismus surgery in terms of postoperative alignment and complications.

Locations
Country Name City State
Pakistan Fauji Foundation Hospital Rawalpindi Punjab

Sponsors (1)
Lead Sponsor Collaborator
Foundation University Islamabad

Country where clinical trial is conducted

Pakistan, 

Outcome
Type Measure Description Time frame Safety issue
Primary Post-operative alignment The post-operative alignment at 1 year will be measured and compared with the pre-operative alignment (deviation) to assess success rate. 1 year
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