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临床试验/CTRI/2025/09/094021
CTRI/2025/09/094021尚未招募4 期

Comparative Evaluation of Laser assisted Ablative Versus Non-ablative Gingival Depigmentation : A Rabdomized Clinical Trial

Saraswati Dental College & Research Centre1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2025年9月12日最近更新:

试验速览

阶段
4 期
状态
尚未招募
发起方
入组人数
30
试验地点
1
主要终点
clinician reported outcomes (Dummet-Gupta oral pigmentation Index, Melanin Index, Gingival Pigmentation Index

研究概览

简要总结

The present split-mouth, prospective, single-centered, parallel group, non-placebo control, double- blinded (investigator and observer) simple randomized comparative clinical trial was conducted in the Department of Periodontology, Saraswati Dental College and Hospital, Lucknow, between April 2023 to December 2024. The study design and protocol were conducted in accordance with ethical principles laid down in Helsinki declaration 1998 revised 2013. After approval from Institutional Research and Development Committee (SDC/IRDC/2022/MDS/13) and Institutional Human Ethical Committee (SDC&H/IHEC/2022/MDS/13), all the participants were informed about the study and written informed consent were obtained from the patients in patient’s vernacular language.

研究设计

研究类型
Interventional
分配方式
Coin toss, Lottery, toss of dice, shuffling cards etc
盲法
Investigator Blinded

入排标准

年龄范围
18.00 Year(s) 至 35.00 Year(s)(—)
性别
All

入选标准

  • 18 to 35 years of age.

排除标准

  • 1.The gingival hyperpigmentation that is secondary as a result of a systemic/ congenital condition/ disorder e.g. McCune Albright syndrome, Hutchinson Gilford Progeria Syndrome, Dyskeratosis congentia, Familial Progressive hyperpigmentation etc.
  • Participants with gingival hyperpigmentation due to the use of medications e.
  • tetracycline.
  • Participants who were chronic smokers (self-reported)
  • Participants contraindicated for laser therapy (with phototoxicity, oral malignancy).

结局指标

主要结局

clinician reported outcomes (Dummet-Gupta oral pigmentation Index, Melanin Index, Gingival Pigmentation Index

时间窗: Baseline, 1 week, 1 month and 3 months.

次要结局

  • Patient Post Surgical Discomfort Score, Patient Satisfaction Score, Patient Esthetic Score(Baseline, 1 week, 1 month and 3 month)
  • Patient Post Surgical Discomfort Score (PPSDS), Patient Esthetic Score (PES), Patient Satisfaction Score (PSS)(PPSDS- 24 hours after intervention)

研究者

发起方
Saraswati Dental College & Research Centre
申办方类型
Research institution and hospital
责任方
Principal Investigator
主要研究者

Shruti Singh

Saraswati Dental College and Hospital

研究点 (1)

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