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To Study The Efficacy of Kalonji Vati With Krishnatil Kwath Ghanvati in Oligohypomenorrhoea

Randomized Comparative Clinical Study of Kalonji Vati With Krishnatil Kwath Ghanvati in Artavkshaya W.S.R. to Oligohypomenorrhoea

Status
Recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/05/052226
Enrollment
70
Registered
2023-05-02
Start date
Unknown
Completion date
Unknown
Last updated
2023-11-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: N915- Oligomenorrhea, unspecified

Interventions

None listed

Sponsors

Dr Mitali Dhaval Malgave
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 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

Exclusion criteria

Exclusion criteria: 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 • Lactating woman • Woman having IUCD • PCOD With metabolic syndrome 4. Intermenstrual duration more than 60 days

Design outcomes

Primary

MeasureTime frame
To evaluate the effect of Kalonji Vati and Krishnatil Kwath Ghanvati in Artavakshaya W.S.R. to OligohypomenorrhoeaTimepoint: 16 weeks

Secondary

MeasureTime frame
1.To study in detail the Nidana Samprapti of Artavakshaya. 2.To study etiopathology of oligohypomenorrhoea.Timepoint: 12 weeks

Countries

India

Contacts

Public ContactDr Mitali Dhaval Malgave

Yashwant Ayurvedic college, post graduate training and research centre,Kodoli, TAL:Panhala

vishalaturlapati@gmail.com9960217429

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026