To Study The Efficacy of Kalonji Vati With Krishnatil Kwath Ghanvati in Oligohypomenorrhoea
- Conditions
- Health Condition 1: N915- Oligomenorrhea, unspecified
- Registration Number
- CTRI/2023/05/052226
- Lead Sponsor
- Dr Mitali Dhaval Malgave
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
1.All female Patients in the Age group of 18-35 yrs (married , unmarried ,
nulliparous, parous, multiparous ) who are willing to participate in the study
who are having symptoms of oligohypomenorrhoea.
2. Female patients irrespective of caste , income group and any occupation will be
selected
3.lntermenstrual duration more than 35 days
4.Menstrual bleeding flow less than 2 days.
5.BMI – 18-30
6.Clinically diagnosed K/C/O PCOD without metabolic syndrome.
7.All Patients who are having symptoms of Artavakshaya i.e. Yathochitkal Adarshan,
Alpata (Reduce Quntity as well as duration ),Yonivedana
1.Major systemic disease likely to influence menstrual cycle like HTN , DM , TB , HIV ,
Thyroid Disorder, Renal Disorders.
2.All dignosed K/C/O malignancy , cervical erosion , polyp , adenomyosis ,
Endometriosis, tubo ovarian mass, Pelvic inflammatory disease.
3.All dignosed K/C/O Premature Ovarian Failure
• HB <9 gm %
• Lactating woman
• Woman having IUCD
• PCOD With metabolic syndrome
4. Intermenstrual duration more than 60 days
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate the effect of Kalonji Vati and Krishnatil Kwath Ghanvati in <br/ ><br>Artavakshaya W.S.R. to OligohypomenorrhoeaTimepoint: 16 weeks
- Secondary Outcome Measures
Name Time Method 1.To study in detail the Nidana Samprapti of Artavakshaya. <br/ ><br>2.To study etiopathology of <br/ ><br>oligohypomenorrhoea.Timepoint: 12 weeks