Treatment of presbyopia with conductive keratoplasty®: Six-month results of the 1-year United States FDA clinical trial

Cornea

Volumn 23, Issue 7, 2004, Pages 661-668

  McDonald, Marguerite B ^a   Durrie, Daniel ^b   Asbell, Penny ^c   Maloney, Robert ^d   Nichamin, Louis ^e  

^a Southern Vision Institute   (United States)

^b Durrie Vision   (United States)

^c MOUNT SINAI MEDICAL CENTER   (United States)

^d Maloney Vision Institute   (United States)

^e Laurel Eye Clinic   (United States)

Author keywords

CK; Conductive keratoplasty; Hyperopia; Presbyopia; Refractive surgery; Thermokeratoplasty

Indexed keywords

ACCOMMODATION; ADULT; AGED; ARTICLE; ASTIGMATISM; CLINICAL TRIAL; CONDUCTIVE KERATOPLASTY; DEVICE; EYE REFRACTION; FEMALE; FOOD AND DRUG ADMINISTRATION; HUMAN; HYPERMETROPIA; KERATOMILEUSIS; KERATOPLASTY; MAJOR CLINICAL STUDY; MALE; MULTICENTER STUDY; PATIENT SATISFACTION; PRESBYOPIA; PRIORITY JOURNAL; REFRACTIVE SURGERY; SAFETY; TREATMENT OUTCOME; VISION; VISUAL ACUITY;

ACCOMMODATION, OCULAR; AGED; COLLAGEN; CORNEAL STROMA; HUMANS; LASERS; MIDDLE AGED; PATIENT SATISFACTION; PRESBYOPIA; PROSPECTIVE STUDIES; STRABISMUS; TIME FACTORS; VISION, BINOCULAR; VISION, MONOCULAR; VISUAL ACUITY;

EID: 4744361807     PISSN: 02773740     EISSN: None     Source Type: Journal    
DOI: 10.1097/01.ico.0000126321.13143.a0     Document Type: Article

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