跳至主要内容
临床试验/CTRI/2024/06/069317
CTRI/2024/06/069317尚未招募Phase 3 4

A Randomized comparative clinical trial to evaluate the efficacy of bharangyadi taila nasya and shadabindu taila nasya with Chitrak haritaki avaleha in kaphaja shiroroga with special reference to chronic maxillary sinusitis

未提供1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2024年7月15日最近更新:

试验速览

阶段
Phase 3 4
状态
尚未招募
入组人数
60
试验地点
1
主要终点
Symptomatic relief

研究概览

简要总结

A randomized clinical trial to evaluate the efficacy of bharangyadi taila nasya and shadbindu taila nasya with Chitrakoot haritaki avaleha in kaphaja Shiro roga w.s.r. to chronic maxillary sinusitis

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
None

入排标准

年龄范围
16.00 Year(s) 至 70.00 Year(s)(—)
性别
All

入选标准

  • Heaviness in head along with dull pain and numbness (guru gauravyukta)
  • Feeling of the head being covered with wet cloth (kaphalipta).
  • Sticky mucus secretion in throat (kaphopadigdhamiti)
  • Headache is less severe than acute sinusitis.
  • Nasal obstruction.
  • Nasal and Post nasal purulent discharge.
  • Facial pain and pressure.
  • Disturbance of smell (hyposmia or anosmia).
  • Patient with chronic maxillary sinusitis were included.
  • Age from 16 years to 70 years.

排除标准

  • Patient not willing for the trial were excluded.
  • Patient with acute maxillary sinusitis were excluded.
  • Pregnant women.
  • Lactating women.
  • Patient suffering from Gastritis with sensitive stomach.
  • Patient suffering from diabetes
  • Patient aged below 16 years and above 70 years.
  • Patients suffering from headache of all other causes except Chronic maxillary sinusitis.
  • Patient suffering from cellulitis of cheek and nasal furuncle.
  • Patient with malignancy of sinuses.

结局指标

主要结局

Symptomatic relief

时间窗: 30 days trial

Prevention of recurrence

时间窗: 30 days trial

次要结局

  • Relief in complications(Reduced quality of life)

研究者

发起方
未提供
责任方
Principal Investigator
主要研究者

Shital Chaudhari

National Institute of Ayurveda, Jaipur.

研究点 (1)

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