TCTR20260726012进行中（未招募）4 期
Hyaluronic acid filler for lip enhancement: a personalized approach based on Asian aesthetic preferences
Thanya Techapichetvanich0 个研究点目标入组 30 人开始时间: 2026年8月3日最近更新:
适应症
试验速览
- 阶段
- 4 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 30
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
- 年龄范围
- 18 Years 至 60 Years（—）
- 性别
- All
入选标准
- •aged 18-60 years
- •Patients with very thin to thin lips
排除标准
- •Participants with permanent facial implants below the subnasal region (e.g., polymethyl methacrylate [PMMA], silicone, or polytetrafluoroethylene [PTFE]).
- •Participants who have previously undergone autologous fat grafting or calcium hydroxyapatite (CaHA) injections below the subnasal region.
- •Participants who have received semi-permanent dermal fillers (e.g., poly-L-lactic acid [PLLA]) below the subnasal region within 6 months prior to enrolment, or temporary dermal fillers within 3 months prior to enrolment.
- •Participants who have received botulinum toxin injections within 6 months prior to enrolment or who plan to undergo botulinum toxin treatment during the study period.
- •Participants who have undergone skin resurfacing procedures, including laser therapy, radiofrequency, ultrasound-based treatments, or chemical peels, within 6 months prior to enrolment or who plan to undergo such procedures during the study period.
- •Participants who have received mesotherapy within 3 months prior to enrolment or who plan to undergo mesotherapy during the study period.
- •Participants with a history of hyaluronic acid dermal filler injection to the lips prior to enrolment.
- •Participants who have undergone thread lifting within 6 months prior to enrolment.
- •Participants who have undergone or are scheduled to undergo orthodontic treatment or dental procedures involving the oral region (e.g., tooth extraction) within 1 month prior to enrolment or during the study period.
- •Participants currently receiving anticoagulant therapy.
- •Participants who have taken non-steroidal anti-inflammatory drugs (NSAIDs), traditional herbal medicines, or other herbal products known to affect blood coagulation within 10 days prior to treatment.
- •Participants with active infection, inflammation, scars, or other lesions involving the lips or perioral region that may interfere with efficacy assessment.
- •Participants with a history of porphyria.
- •Participants with tattoos, piercings, or scars involving the lips or perioral region that may interfere with study assessments.
- •Participants with a known hypersensitivity or allergy to hyaluronic acid or its components.
- •Participants with a history of cardiac conduction abnormalities, hepatic disease, renal disease, or autoimmune disorders.
- •Participants who are pregnant, planning to become pregnant, or breastfeeding.
研究者
相似试验
Unknown
不适用
一项评价 PRECISE-HA Filler LIPS 在中国人群中用于改善嘴唇饱满度和形状时的安全性及有效性的前瞻性、多中心、分层区组随机、不完整设盲、平行阳 性对照临床试验ChiCTR2500096387法国 SYMATESE SAS 公司
尚未招募
3 期
Comparing Hyaluronic Acid Gel and Vitamin E for Healing After Gum Laser Treatment: A clinical studyCTRI/2024/05/067185Dr Samiksha Mandavkar48
招募中
不适用
Functional and Aesthetic Outcomes Following Lower Lip ReconstructionCancerNCT07298070Hôpital NOVO20
尚未招募
4 期
A randomised study comparing clonidine and adrenaline added to lignocaine for blood pressure stability and pain relief during lower molar tooth extraction.CTRI/2025/07/092118Kothiwal Dental College and resaearch centr74
尚未招募
不适用
Effect of test product on lipCTRI/2024/09/073279Vedistry Pvt Ltd.36