Surgical dose response of bilateral medial rectus recession in acquired comitant esotropia compare to infantile esotropia

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

TCTR

Registry ID

TCTR20190401001

Enrollment

300

Registered

2019-04-01

Start date

2019-03-14

Completion date

Unknown

Last updated

2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acquired esotropia and infantile esotropia Acquired esotropia&#44

Interventions

Patients with acquired esotropia who underwent bilateral medial rectus recession,Patients with infantile esotropia who underwent bilateral medial rectus recession

Treatment,Treatment

Acquired esotropia,Infantile esotropia

Eligibility

Sex/Gender

All

Age

0 Years to 45 Years

Inclusion criteria

Inclusion criteria: Patients with acquired comitant esotropia or infantile esotropia who underwent bilateral medial rectus recession.

Exclusion criteria

Exclusion criteria: Additional procedure in the same surgery with bilateral medial rectus recession. Follow up period less than 1 month

Design outcomes

Primary

Measure	Time frame
Surgical dose response at 1 month postoperative prism diopters per millimeter of bilateral medial rectus recession	—

Secondary

Measure	Time frame
Success rate at last visit percentage of success	—

Countries

Thailand

Contacts

Public ContactParnchat Pukrushpan

Chulalongkorn University

parnchat.p@chula.ac.th6622564142

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026