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临床试验/CTRI/2024/05/067959
CTRI/2024/05/067959尚未招募不适用

An observational study to determine the possible association between specific yakkai ilakkanam (Siddha somatotype) in patients with Abnormal uterine bleeding Perumbadu

未提供1 个研究点 分布在 1 个国家目标入组 220 人开始时间: 2024年5月27日最近更新:

试验速览

阶段
不适用
状态
尚未招募
入组人数
220
试验地点
1
主要终点
The possible association of Dhegi characterization in Perumbadu patients will be obtained.

研究概览

简要总结

**PRIMARY OBJECTIVE:**·       To determine the possible association of specific disease uterine bleeding (Perumbadu) on the basis of Dhegi characterisation.

SECONDARY OBEJECTIVE:  To study the relationship of panchapatchi calculation with perumbadu in the subjects included in the research.  To document the specific siddha diagnostic methodology naadi in the subjects.

Study type: An Observational study,**Study design:**Cross sectional study- Case control study

**INCLUSION CRITERIA :**Age :18-55 years. Subject is assessed with PBAC for abnormal uterine bleeding with the following conditions- Fibroid uterus, Adenomyosis, Pelvic endometriosis, Dysfunctional uterine bleeding, Chronic tubo ovarian mass, Endocrinal - hypothyroid and hyperthyroid, Hematological cause and other causes and are included in the study.

EXCLUSION CRITERIA

·Patient not willing to sign the consent form

· Patients with any serious system illness

·Metrorrhagia

PRIMARY OUTCOME:

·       The possible association of Dhegi characterization in Perumbadu patients will be obtained.

SECONDARY OUTCOME

·       The Naadi in the subjects of the study  will be documented.

·       The affected humors in the subjects will be evaluated through the panchapatchi calculation

RESULTS AND DISCUSSION: The results will be statistically analysed and reported.

KEY WORDS: Dhegi, Yakkai ilakkanam, Siddha,  Perumbadu, Abnormal uterine bleeding.

研究设计

研究类型
Observational

入排标准

年龄范围
18.00 Year(s) 至 55.00 Year(s)(—)
性别
Female

入选标准

  • Subject is assessed with PBAC for abnormal uterine bleeding with the following conditions- Fibroid uterus, Adenomyosis, Pelvic endometriosis, Dysfunctional uterine bleeding, Chronic tubo ovarian mass, Endocrinal.
  • hypothyroid and hyperthyroid, Hematological cause and are included in the study.

排除标准

  • Patient not willing to sign the consent form Patients with any serious system illness Metrorrhagia.

结局指标

主要结局

The possible association of Dhegi characterization in Perumbadu patients will be obtained.

时间窗: 18 months

次要结局

  • The Naadi in the subjects of the study will be documented.(The affected humors in the subjects will be evaluated through the panchapatchi calculation.)

研究者

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

KOUSALYA S

National Institute of Siddha

研究点 (1)

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