跳至主要内容
临床试验/CTRI/2026/02/103760
CTRI/2026/02/103760尚未招募不适用

Comparative evaluation of mouthwash containing 0.1% Hydrogen Peroxide, 0.05% lactoferrin and 0.14% zinc lactate with 2% povidone iodine on clinical healing outcomes following periodontal surgery A Randomised controlled trial

GROUP PHARMACEUTICALS1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2026年3月2日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
20
试验地点
1

研究概览

简要总结

This study aims to compare the effect of two postoperative mouthwashes on healing after periodontal surgery. One mouthwash contains 0 point 1 percent hydrogen peroxide 0 point 05 percent lactoferrin and 0 point 14 percent zinc lactate and the other contains 2 percent povidone iodine. Twenty systemically healthy patients with stage three grade B periodontitis who require periodontal surgery will be included in the study. Patients will be randomly divided into two groups using computer generated randomization. The study will follow a double blinding method where both the patient and examiner will not know which mouthwash is given. The mouthwashes will be dispensed in coded amber bottles. Patients will use the assigned mouthwash for twenty one days after surgery. Clinical healing will be evaluated using healing index and patient pain will be assessed using visual analogue scale at baseline and after twenty one days. The results of this study may help in selecting an effective postoperative mouthwash for better periodontal healing outcomes.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant and Investigator Blinded

入排标准

年龄范围
35.00 Year(s) 至 55.00 Year(s)(—)
性别
All

入选标准

  • Patients aged 35 to 55 years Systemically healthy patients Diagnosed with stage three grade B periodontitis Completed nonsurgical periodontal therapy at least three months before surgery Indicated for periodontal flap surgery without regenerative procedures Non smokers Patients willing to participate and provide informed consent.

排除标准

  • Patients with systemic diseases affecting wound healing such as diabetes mellitus or severe anemia Patients who used systemic antibiotics in last six months Patients taking medications affecting healing such as corticosteroids or cytotoxic drugs Smokers Pregnant or breastfeeding women Patients requiring regenerative periodontal surgery Patients not willing to follow study protocol.

研究者

发起方
GROUP PHARMACEUTICALS
申办方类型
Pharmaceutical industry-Indian
责任方
Principal Investigator
主要研究者

DR SUJAY J

AJ INSTITUTE OF DENTAL SCIENCES

研究点 (1)

Loading locations...

相似试验