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临床试验/CTRI/2025/07/091389
CTRI/2025/07/091389尚未招募2/3 期

Evaluation of comparative efficacy of Navana Nasya with Shadbindu Ghrita versus 0.1 percent Xylometazoline - Hydrochloride nasal drop in the management of Vataj Pratishyaya (Allergic Rhinitis): Randomized Controlled Trial

Dr Darpan Madhao Borkar1 个研究点 分布在 1 个国家目标入组 56 人开始时间: 2025年8月27日最近更新:

试验速览

阶段
2/3 期
状态
尚未招募
发起方
入组人数
56
试验地点
1
主要终点
1. To assess the efficacy of navan nasya with shadbindu ghrita on TNSS and DNE in Vataj Pratishaya (Allergic rhinitis)

研究概览

简要总结

This study, titled Evaluation of comparative efficacy of Navana Nasya with Shadbindu Ghrita versus 0.1 percent Xylometazoline - Hydrochloride nasal drop in the management of Vataj Pratishyaya (Allergic Rhinitis) Randomized Controlled Trial, aims to compare an Ayurvedic nasal treatment with a modern nasal spray for allergic rhinitis. The research is important because while modern medicines offer quick relief, they can have side effects with long-term use, and there’s a lack of comparative studies for Ayurvedic alternatives. This study will involve 56 patients divided into two groups, receiving either the Ayurvedic treatment or Xylometazoline nasal drops for 7 days. The effectiveness will be measured using TNSS and DNE scores after 14 days to see if the Ayurvedic treatment is as effective as the modern nasal spray.

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研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant Blinded

入排标准

年龄范围
18.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • A patient who is willing to take part and provides signed informed consent, Patient having vataj Pratishyaya will be randomly selected, Selection is irrespective of gender, religion & socio economical class.

排除标准

  • Patients having Lower respiratory tract infections, Atrophic Rhinitis, C.S.F Rhinorrhoea and any other systemic disease, recently operated patients (Nose cases), In lactating and pregnant women.

结局指标

主要结局

1. To assess the efficacy of navan nasya with shadbindu ghrita on TNSS and DNE in Vataj Pratishaya (Allergic rhinitis)

时间窗: 1. Baseline (Day 0)- assessment of TNSS and DNE scores before intervention in both groups | 2. Post-intervention (Day 14)- Reassessment of TNSS and DNE scores after completion of treatment in both groups.

2. To assess the efficacy of 0.1 percent Xylometazoline Hydrochloride nasal drop on TNSS and DNE in Vataj Pratishaya (Allergic rhinitis)

时间窗: 1. Baseline (Day 0)- assessment of TNSS and DNE scores before intervention in both groups | 2. Post-intervention (Day 14)- Reassessment of TNSS and DNE scores after completion of treatment in both groups.

3. To compare the efficacy navan nasya with shadbindu ghrita and 0.1 percent Xylometazoline Hydrochloride nasal drop on TNSS and DNE in Vataj Pratishaya

时间窗: 1. Baseline (Day 0)- assessment of TNSS and DNE scores before intervention in both groups | 2. Post-intervention (Day 14)- Reassessment of TNSS and DNE scores after completion of treatment in both groups.

(Allergic rhinitis)

时间窗: 1. Baseline (Day 0)- assessment of TNSS and DNE scores before intervention in both groups | 2. Post-intervention (Day 14)- Reassessment of TNSS and DNE scores after completion of treatment in both groups.

次要结局

未报告次要终点

研究者

发起方
Dr Darpan Madhao Borkar
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Dr Darpan Madhao Borkar

Mahatma Gandhi Ayurved College Hospital and Research Centre Salod Hirapur Wardha

研究点 (1)

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