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Ocular photobiomodulation therapy for visual rehabilitation after retinal detachment surgery

Ocular photobiomodulation therapy for visual rehabilitation after retinal detachment surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300078628
Enrollment
Unknown
Registered
2023-12-14
Start date
2023-12-30
Completion date
Unknown
Last updated
2023-12-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Rhegmatogenous retinal detachment

Interventions

Group A:Photobiomodulation therapy
Group B:None

Sponsors

Chongqing Aier Eye Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) patients with simple rhegmatogenous retinal detachment and retinal reattachment at 1 month after surgery. (2) Age from 18 to 70 years old, regardless of gender. (3) patients who met the diagnostic criteria of primary rhegmatogenous retinal detachment and underwent surgical treatment in the two hospitals. One month after surgery, the corrected visual acuity was between 0.02 and 0.3. (4) There was no obvious opacity of the refractive stroma. (5) The subjects voluntarily joined the study and signed the informed consent form, with good compliance and cooperation with treatment and follow-up.

Exclusion criteria

Exclusion criteria: (1) combined with other ocular diseases that affect vision, such as diabetic retinopathy, traumatic retinopathy, glaucoma, optic atrophy, etc. (2) Mental illness and communication disorders, unable to cooperate or unwilling to cooperate. (3) pregnant women and children. (4) complicated with important organ dysfunction, malignant tumor, hematological diseases and recent history of major diseases. (5) other conditions considered by the investigators to be inappropriate for participation in the trial. (6) Participants who participated or were participating in other clinical trials within 3 months before enrollment. (7)The natural pupil diameter in a dark room is greater than 4mm.

Design outcomes

Primary

MeasureTime frame
Best corrected visual acuity;

Secondary

MeasureTime frame
Continuity of Ellipsoid zone;mf- ERG;Subfoveal choriocapillaris flow density;Foveal retinal capillary plexus flow density;

Countries

China

Contacts

Public ContactYi Wang

Chongqing Aier Eye Hospital

wangyieye@aliyun.com+86 138 0835 3062

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026