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临床试验/CTRI/2025/10/095774
CTRI/2025/10/095774尚未招募不适用

Study of premenstrual syndrome and its management from synthesis repertory using PMSS scale

Dr Urvi Makwana1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2025年10月21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
50
试验地点
1
主要终点
Improvement in PMSS scale before and after treatment

研究概览

简要总结

Premenstrual Syndrome (PMS) is a common cyclic disorder affecting women of reproductive age, characterized by physical, emotional, and behavioral symptoms occurring in the luteal phase of the menstrual cycle and subsiding with menstruation. The Premenstrual Syndrome Scale (PMSS) is a standardized, self-report instrument used to assess the severity and frequency of PMS symptoms across multiple domains, including psychological (irritability, anxiety, depression), physical (bloating, breast tenderness, headache), and behavioral changes (sleep disturbances, appetite changes, social withdrawal).

Research using the PMSS aims to:

Quantify prevalence and severity of PMS among study populations.

Identify symptom patterns and dominant clusters across different demographic and clinical groups.

Evaluate associations with lifestyle, stress, diet, and comorbidities.

Assess treatment efficacy (pharmacological, homoeopathic, or lifestyle interventions) by comparing pre- and post-intervention PMSS scores.

The PMSS thus provides a reliable, multidimensional tool for both clinical assessment and research, facilitating early identification, proper management, and evaluation of outcomes in women experiencing PMS.

研究设计

研究类型
Interventional

入排标准

年龄范围
14.00 Year(s) 至 45.00 Year(s)(—)
性别
Female

入选标准

  • Women diagnosed with premenstrual syndrome (PMS).
  • Age group: typically women aged 14-45 years No history of other gynaecological disorders or serious comorbidities that could affect PMS symptoms.

排除标准

  • Exclusion criteria:- Women with severe psychiatric disorders (eg schizophrenia, bipolar disorder).
  • Women undergoing hormonal therapy or other medications that could interfere with PMS symptoms.
  • • Women aged before 14 and after
  • • Women with other gynaecological disease ,pregnancy, or breast feeding women.

结局指标

主要结局

Improvement in PMSS scale before and after treatment

时间窗: Before and after treatment

次要结局

  • Improvement in PMSS scale before and after treatment(Every follow up like 15th day, 1 month...)

研究者

发起方
Dr Urvi Makwana
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Dr Urvi Makwana

Anand Homoeopathic Medical College and Research Institute

研究点 (1)

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