→ 目の見えない人、目の不自由な人、視覚障害者

→ 目の見えない、目の不自由な、視覚障害のある

→ やみくもに、でたらめに

An institution for blind or deaf children shall be a facility intended for admitting and protecting blind children （including severely amblyopic children） or deaf children （including severely cloth-eared children）, and providing guidance or assistance necessary for independent and self-supporting life to them.〔【出典】日本法令外国語訳データベースシステム 〕

blind screening

blind lancet

blind lancet arch

a school for the blind, deaf and other disabled

blind loop

pocket epithelium

pocket formation

blind sac-like structure

blind pouch syndrome

blind student

blinding glare

fire at random

blind patch《工学》

Data monitoring without code-breaking should also be described, even if this kind of monitoring is considered to cause no increase in type I error.〔【出典】ICHガイドライン 〕

If the blind review suggests changes to the principal features stated in the protocol, these should be documented in a protocol amendment.〔【出典】ICHガイドライン 〕

If blinding was considered desirable but not feasible, the reasons and implications should be discussed.〔【出典】ICHガイドライン 〕

Use of a blinded placebo control may decrease the amount of improvement resulting from subject or investigator expectations because both are aware that some subjects will receive no active drug.〔【出典】ICHガイドライン 〕

If there was a data monitoring committee with access to unblinded data, procedures to ensure maintenance of overall study blinding should be described.〔【出典】ICHガイドライン 〕

The essential aim is to prevent identification of the treatments until all such opportunities for bias have passed.〔【出典】ICHガイドライン 〕

Blinding is intended to ensure that subjective assessments and decisions are not affected by knowledge of treatment assignment.〔【出典】ICHガイドライン 〕

Blinding is intended to minimize the potential biases resulting from differences in management, treatment, or assessment of patients, or interpretation of results that could arise as a result of subject or investigator knowledge of the assigned treatment.〔【出典】ICHガイドライン 〕

Blinding is an important means of reducing or minimising the risk of biased study outcomes.〔【出典】ICHガイドライン 〕

Blinding or masking is intended to limit the occurrence of conscious and unconscious bias in the conduct and interpretation of a clinical trial arising from the influence which the knowledge of treatment may have on the recruitment and allocation of subjects, their subsequent care, the attitudes of subjects to the treatments, the assessment of end-points, the handling of withdrawals, the exclusion of data from analysis, and so on.〔【出典】ICHガイドライン 〕

This concern may be particularly relevant in cross-over studies.〔【出典】ICHガイドライン 〕

Such problems or potential problems should be identified and if there were any attempts to assess the magnitude of the problem or manage it （e.g., by having some endpoint measurements carried out by people shielded from information that might reveal treatment assignment）, they should be described.〔【出典】ICHガイドライン 〕

The procedures, including means of maintaining blindness, and centralising readings and measurements, should be described fully.〔【出典】ICHガイドライン 〕

blind trial《医》

blind clinical trial

Any changes in the analysis made after blind-breaking should be identified.〔【出典】ICHガイドライン 〕

blind study

blind fistula

blindfold go《囲碁》〔「めくら」は差別語。〕

blank ［false］ window

blind-ending vagina

blind-loop syndrome

blindsight《医》

blindsight person

blind valley

blind trade〔「めくら」は差別語〕

blind axle

carry out a randomized, placebo-controlled, double-blind trial of