Head Positioning After Retina Detachment Repair
Part of paid clinical trials in Prairie Village, Kansas.
- Sponsor
- University of Kansas Medical Center
- Study ID
- NCT03714503
- Status
- Recruiting
Conditions
- Retina; Detachment, Rhegmatogenous
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Retina re-attachment repair using C3F8 gas tamponade — DEVICEAssigning a one day post-operative head positioning
Study Details
This study aims to determine if one day post-operative prone head positioning can be as good as seven days post-operative prone head positioning in patients with retinal detachments with inferior retinal breaks after pars that pars plana vitrectomy (PPV) using perfluoropropane (C3F8) gas as a tamponade. The investigator will conduct a single arm phase II study using a Simon's two-stage design
Key Dates
- Start date
- Apr 8, 2019
- Status verified
- Apr 2026
- Primary completion
- Dec 31, 2028
- Completion
- Dec 31, 2028
Study Design
- Enrollment
- 20 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- HEALTH_SERVICES_RESEARCH
Arms
- Other: One day post-operative head positioningpatients will be assigned to remain a one-day post operative head positioning following retina re-attachment surgery
Primary Outcome Measure
Retina attachment on clinical exam using the indirect ophthalmoscope [ Time Frame: 3 months ]
Central Contacts
- Ariana Madrigal9135880105
- Abby Strickland913-588-6600
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of Kansas Medical Center | Prairie Village | Kansas | 66208 | Abby Strickland Radwan S Ajlan, MBBCh (PRINCIPAL_INVESTIGATOR) |
Find similar trials in Prairie Village, KS
By research site