CTRI/2024/04/066000招募中4 期
Efficacy and safety of monophasic versus biphasic hyaluronic acid dermal fillers in correction of moderate-to-severe nasolabial folds: A randomized, controlled, double blinded and intraindividual study - NI
Punjab government dental college and hospital Amritsar0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- 4 期
- 状态
- 招募中
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •Male or female, aged 25 years or older, with moderate-to-severe
- •symmetrical NLFs graded 3 (moderate) or 4 (severe) according to the 5-
- •grade Nasolabial Fold- Wrinkle Severity Rating Scale (NLF-WSRS).
- •Patients with healthy facial skin, free of disease or pathology in the area to
- •be treated.
- •Patients willing to abstain from any other facial, surgical or cosmetic
- •procedures in the treatment area for the duration of clinical study.
排除标准
- •Patients with active skin disease, tumors, infection or related condition in or
- •near the area to be treated
- •Patients hypersensitive or allergic to hyaluronic acid, lidocaine or any amide
- •type of anesthetic.
- •Patients with corrective procedures performed or planned in nasolabial
- •region, such as silicone implants, permanent or semi-permanent fillers, laser
- •therapy, dermabrasion, botulinum toxin application, chemical peeling within
- •one year of the study.
- •Patients who are pregnant, lactating or on oral contraceptives.
- •Patients with tendency to hypertrophic scars, keloid formation, pigmentation
- •disorders, any autoimmune or connective tissue disorders.
- •Patients with diabetes mellitus, uncontrolled systemic diseases and on
- •antiplatelet, anticoagulant or thrombolytic medications.
- •Patients with mental disorders or emotional instability.
- •Patients who’ll not give consent for the procedure.
研究者
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