Trials / Completed
CompletedNCT00120445
Comparison of Air and Expansile Gas in Pneumatic Retinopexy
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 126 (actual)
- Sponsor
- Khon Kaen University · Academic / Other
- Sex
- All
- Age
- —
- Healthy volunteers
- Not accepted
Summary
The objective of the study is to evaluate the results of using air versus expansile gas (perfluoropropane) in the treatment of rhegmatogenous retinal detachment by pneumatic retinopexy, comparing the retinal reattachment rate and post-operative visual recovery.
Detailed description
To the best of the investigators' knowledge there have been no clinical trials to compare air and expansile gas in pneumatic retinopexy. The investigators hypothesize that both air and expansile gas have the same properties of gas and remain in the eye for 5-6 days which is long enough to have moderate chorioretinal adhesion to seal the retinal break. If the investigators can prove that air is equivalent to expansile gas in this procedure, it can save a lot of money for the country. Therefore, the investigators are conducting a randomised controlled double-blind study to compare the results of using air and perfluoropropane in pneumatic retinopexy for treatment of rhegmatogenous retinal detachment.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | air | 0.3 ml of filtered air |
| PROCEDURE | expansile gas | 0.3 ml of perfluoropropane gas |
Timeline
- Start date
- 2004-07-01
- Completion
- 2007-10-01
- First posted
- 2005-07-18
- Last updated
- 2012-03-09
Locations
1 site across 1 country: Thailand
Source: ClinicalTrials.gov record NCT00120445. Inclusion in this directory is not an endorsement.