RAMP Trial Design
Cross-source consensus on RAMP Trial Design from 1 sources and 5 claims.
1 sources · 5 claims
Comparisons
Other
Other
Highlighted claims
- RAMP is a prospective multicentre randomised controlled trial with 12 months of follow-up. — LED red light for atrophy and microcirculation in pathologic myopia (RAMP): study design and protocol for a multicentre randomised controlled trial
- The study plans to enrol 158 adults with pathologic myopia aged 18-55 years. — LED red light for atrophy and microcirculation in pathologic myopia (RAMP): study design and protocol for a multicentre randomised controlled trial
- Participants are randomly assigned in a 1:1 ratio to active RLRL or sham control, with 79 participants in each arm. — LED red light for atrophy and microcirculation in pathologic myopia (RAMP): study design and protocol for a multicentre randomised controlled trial
- Recruitment began on 31 December 2025 and the full study is expected to end by 30 December 2028. — LED red light for atrophy and microcirculation in pathologic myopia (RAMP): study design and protocol for a multicentre randomised controlled trial
- The sham control devices look identical and emit the same 660 nm wavelength at a non-therapeutic power density. — LED red light for atrophy and microcirculation in pathologic myopia (RAMP): study design and protocol for a multicentre randomised controlled trial