Controlled, randomized study of pain levels in subjects treated with calcium hydroxylapatite premixed with lidocaine for correction of nasolabial folds

Dermatologic Surgery

Volumn 36, Issue 3, 2010, Pages 309-315

  Marmur, Ellen ^a   Green, Lawrence ^b   Busso, Mariano ^c  

^a MOUNT SINAI MEDICAL CENTER   (United States)

^b GEORGE WASHINGTON UNIVERSITY SCHOOL OF MEDICINE AND HEALTH SCIENCES   (United States)

^c UNIVERSITY OF MIAMI   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANESTHETIC AGENT; HYDROXYAPATITE; HYDROXYAPATITE PLUS LIDOCAINE; LIDOCAINE; UNCLASSIFIED DRUG;

ADULT; AGED; ARTICLE; CLINICAL ARTICLE; CLINICAL TRIAL; CONTROLLED CLINICAL TRIAL; CONTROLLED STUDY; DEPRESSION; DRUG EFFICACY; DRUG SAFETY; FACE; FEMALE; HUMAN; MALE; NASOLABIAL FOLD; PAIN ASSESSMENT; PIMPLE; PRIORITY JOURNAL; PRURITUS; RANDOMIZED CONTROLLED TRIAL; SINGLE BLIND PROCEDURE; SKIN BLEEDING; SKIN BRUISING; SKIN MANIFESTATION; SKIN PAIN; SKIN REDNESS; SKIN SWELLING; VISUAL ANALOG SCALE;

ADULT; AGED; AGED, 80 AND OVER; ANESTHETICS, LOCAL; BIOCOMPATIBLE MATERIALS; COSMETIC TECHNIQUES; DRUG COMBINATIONS; DURAPATITE; FACE; FEMALE; HUMANS; LIDOCAINE; MALE; MIDDLE AGED; PAIN, POSTOPERATIVE; PROSPECTIVE STUDIES; SINGLE-BLIND METHOD;

EID: 77749234170     PISSN: 10760512     EISSN: 15244725     Source Type: Journal    
DOI: 10.1111/j.1524-4725.2009.01435.x     Document Type: Article

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