Trials / Unknown
UnknownNCT03381079
Efficacy and Safety of Posterior Scleral Reinforcement on Controlling Myopia in Adults With High Myopia
Posterior Scleral Reinforcement for Adults With High Myopia
- Status
- Unknown
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 120 (estimated)
- Sponsor
- Beijing Tongren Hospital · Academic / Other
- Sex
- All
- Age
- 18 Years – 40 Years
- Healthy volunteers
- Not accepted
Summary
This study will evaluate the efficacy and safety of posterior scleral reinforcement on controlling myopia progression, including change in refraction, axial elongation as well as sight-threatening complications, in adults with high myopia. Half the adults will receive posterior scleral reinforcement, while the other half will receive no surgerical treatment.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Posterior scleral reinforcement | Posterior scleral reinforcement (pPSR) is a procedure applied with autologous or biological material or synthetic materials reinforcing pole of the sclera after eyeball, in order to prevent or alleviate myopic development. |
Timeline
- Start date
- 2018-04-01
- Primary completion
- 2020-10-01
- Completion
- 2020-12-31
- First posted
- 2017-12-21
- Last updated
- 2017-12-22
Source: ClinicalTrials.gov record NCT03381079. Inclusion in this directory is not an endorsement.