Study to measure the volume of the Human Eye
Not Applicable
- Conditions
- Health Condition 1: H00-H59- Diseases of the eye and adnexa
- Registration Number
- CTRI/2022/03/041275
- Lead Sponsor
- Sankara Eye Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Inclusion Criteria
1.All patients undergoing pars plana vitrectomy .
2.All patients undergoing silicone oil removal between .
Exclusion Criteria
Exclusion Criteria
1.Patients with past or present suprachoroidal heamorrhage or choroidal detachment not resolving during surgery.
2.Patients with intra-ocular tumors.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. Correlation of vitreous volume with axial length and refractive error <br/ ><br>2. Compare measure volume with volume of oil injectedTimepoint: All outcomes will be assessed at the end of study period of 3 months.
- Secondary Outcome Measures
Name Time Method Compare measure volume with age/sex/refractive error/axial lengthTimepoint: End of study period