跳至主要内容
临床试验/CTRI/2026/01/102436
CTRI/2026/01/102436尚未招募2 期

A Comparative Clinical Study To Evaluate The Efficacy Of Mahanarayana Taila Matrabasti and Shatpushpa Taila Matrabasti In Artavakshaya w.s.r To Endometrial Hypoplasia/Thin Endometrium.

Dr Navneet1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2026年3月20日最近更新:

试验速览

阶段
2 期
状态
尚未招募
发起方
入组人数
40
试验地点
1

研究概览

简要总结

This study is a randomized, comparative, open-label clinical trial designed to evaluate the efficacy of Mahanarayana Taila Matrabasti and Shatpushpa Taila Matrabasti in the management of Artavakshaya with special reference to endometrial hypoplasia/thin endometrium. A total of 40 patients aged 15–40 years, fulfilling diagnostic and inclusion criteria, will be randomly allocated into two groups of 20 each. Group A will receive Mahanarayana Taila Matrabasti and Group B will receive Shatpushpa Taila Matrabasti for 7 days from the 4th day of menstruation for two consecutive cycles. Assessment will be done using subjective menstrual parameters and objective measurement of endometrial thickness. The study duration is 3 months, including follow-up.

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
15.00 Year(s) 至 40.00 Year(s)(—)
性别
Female

入选标准

  • 1 Age between 15 to 40 years irrespective of marital status.
  • 2 Symptoms of artavkshaya yathochitakala adarshan , alpata, yonivedana (any of two) 3 Duration of menses less than 2 days, Quantity less than 2 pad per day and Spotting menses for previous 2 to 3 consecutive cycles 4 Endometrial thickness less than 7mm at the time of Luteal Phase on day 21 of cycle .
  • 5 Patient is willing to participate in study And Give Written consent for the study.

排除标准

  • 1 Peri Menopause & Post Menopause women 2 Patients suffering from Thyroid dysfunction, PCOS diabetes mellitus , severe anemia (less than 8gm/Dl) ,Congenital abnormalities of reproductive system 3 Patient on OC Pills.

研究者

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

Dr Navneet

Parul Institute Of Ayurved

研究点 (1)

Loading locations...

相似试验