European Multicentre Randomised Controlled Clinical Trial: Heavy Silicone Oil versus Standard Silicone Oil as long Term Vitreous Tamponade (HSO-Study).

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON25635

Enrollment

Registered

2005-08-23

Start date

2005-05-01

Completion date

Unknown

Last updated

2024-02-28

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

Conditions

None listed

Interventions

Medical device.

Eligibility

Inclusion criteria

Inclusion criteria: 1. Ablatio retinae with PVR; 2. Giant tear below 10-12 h.

Exclusion criteria

Exclusion criteria: 1. Defects above 10-2 h; 2. Proliferative diabetic retinopathy; 3. Trauma; 4. Uveitis; 5. Glaucoma; 6. Monoculus.

Design outcomes

Primary

Measure	Time frame
Complete retinal reattachment and ETDRS vision after 12 months.	—

Secondary

Measure	Time frame
Number of resurgeries within 12 months.	—

Contacts

Public ContactJ.C. Meurs, van

Oogziekenhuis Rotterdam, Schiedamsevest 180

vanMeurs@oogziekenhuis.nl+31 (0)10 4017777

Outcome results