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Questionnaire Study for Intraoperative Amaurosis Experience under Sub-tenon's Anesthesia

Questionnaire Study for Intraoperative Amaurosis Experience under Sub-tenon's Anesthesia

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900027998
Enrollment
Unknown
Registered
2019-12-08
Start date
2019-12-01
Completion date
Unknown
Last updated
2019-12-10

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

Conditions

vitreoretinal diseases

Interventions

Case series:inquiry about visual experience during surgery

Sponsors

Joint Shantou International Eye Center of Shantou University and the Chinese University of Hong Kong
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. aged 18 to 60 years old; 2. showd good response to the questions by researchers preoperatively; 3. prepared for vitreoretinal surgery or silicone oil removal surgery; 4. Had a preoperative best corrected visual acuity of Hand Movement or better in the diseased eye and 4/200 or better in the contralateral eye; 5. Patients are voluntarily involved in this clinical trial and signed informed consent.

Exclusion criteria

Exclusion criteria: 1. showed difficulties in cooperating with the operators; 2. combined with other vision-threatening eye diseases in the affected eye, including glaucoma, retinal detachment, vitreal hemorrhage, diabetic retinopathy, and retinal neovascularization disease, etc.

Design outcomes

Primary

MeasureTime frame
Experiencing amaurosis;Changes in color;

Secondary

MeasureTime frame
heart beat;blood pressure;

Countries

China

Contacts

Public ContactDezhi Zheng

Joint Shantou International Eye Center of Shantou University and the Chinese University of Hong Kong

zdz@jsiec.org+86 159 8984 9662

Outcome results

None listed

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