Comparative evaluation of diode laser versus argon laser photocoagulation in patients with central serous retinopathy: a pilot, randomised controlled trial
| ISRCTN | ISRCTN84128484 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN84128484 |
| Protocol serial number | N/A |
| Sponsor | All-India Institute of Medical Sciences (AIIMS) (India) |
| Funder | All-India Institute of Medical Sciences (AIIMS) (India) |
- Submission date
- 04/10/2004
- Registration date
- 05/10/2004
- Last edited
- 07/08/2007
- Recruitment status
- No longer recruiting
- Overall study status
- Completed
- Condition category
- Eye Diseases
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data
Plain English summary of protocol
Not provided at time of registration
Contact information
Dr Lalit Verma
Scientific
Scientific
E- 18, Hudco palace
Andrews ganj
New Delhi
110049
India
| lalitverma@yahoo.com |
Study information
| Primary study design | Interventional |
|---|---|
| Study design | Randomised controlled trial |
| Secondary study design | Randomised controlled trial |
| Scientific title | |
| Study objectives | Central Serous Retinopathy (CSR) is a retinal disorder affecting young adults, characterized clinically by a well-defined, translucent, circumscribed detachment of neurosensory retina at the posterior pole, usually involving the macula. The detachment results from accumulation of transparent fluid in the potential space between retinal pigment epithelial layer and the neurosensory retina. Hypothesis: To evaluate the efficacy of diode laser photocoagulation in patients with central serous retinopathy (CSR) and to compare it with the effects of argon green laser. |
| Ethics approval(s) | Not provided at time of registration |
| Health condition(s) or problem(s) studied | Central Serous Retinopathy (CSR) |
| Intervention | 1. Diode Laser photocoagulation 2. Argon green laser photocoagulation 3. Fluorescein Angiography |
| Intervention type | Other |
| Primary outcome measure(s) |
Not provided at time of registration |
| Key secondary outcome measure(s) |
Not provided at time of registration |
| Completion date | 01/06/2000 |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Not Specified |
| Sex | Not Specified |
| Target sample size at registration | 30 |
| Key inclusion criteria | Patients of unilateral type 1 CSR |
| Key exclusion criteria | Not provided at time of registration |
| Date of first enrolment | 01/01/1998 |
| Date of final enrolment | 01/06/2000 |
Locations
Countries of recruitment
- India
Study participating centre
E- 18, Hudco palace
New Delhi
110049
India
110049
India
Results and Publications
| Individual participant data (IPD) Intention to share | No |
|---|---|
| IPD sharing plan summary | Not provided at time of registration |
| IPD sharing plan |
Study outputs
| Output type | Details | Date created | Date added | Peer reviewed? | Patient-facing? |
|---|---|---|---|---|---|
| Results article | Results | 29/10/2004 | Yes | No |
