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Role of Krishnadi churna and Madhutailik basti in PCOS

Effect of Krishnadi churna and Madhutailik Basti in the management of Polycystic Ovarian Syndrome- Clinical Trial and In-silico study - NIL

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/01/079712
Enrollment
66
Registered
2025-01-29
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

Health Condition 1: E282- Polycystic ovarian syndrome

Interventions

None listed

Sponsors

Faculty of Ayurveda Institute of Medical Sciences BHU
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)Female patients of Age group 16 - 40 years. 2)Patients diagnosed with PCOS as defined by Modified Rotterdam Criteria ie if any two of the following are present (i)Clinical(Acne, hirsutism, hairloss) or Biochemical(raised total or free Testosterone ) evidence of hyperandrogenism. (ii) Oligo-Anovulation (Oligo-amenorrhoea (cycles more than 35 days apart or less than 8 menses a year ) (iii)Polycystic Ovarian Morphology ( more than or equal to 20 follicles per ovary in either ovary, more than or equal to 10 cm ovarian volume) 3) Both married and unmarried patients

Exclusion criteria

Exclusion criteria: 1. Patient of age less than 16 and above the age of 40 years. 2. Patients with diagnosed cases of congenital malformation of uterus, adnexa or reproductive organs. 3. Benign and Malignant lesion of reproductive organs. 4. Endocrinal dysfunction like Thyroid Dysfunction, Adrenal Hyperplasia. 5. Women with chronic ailments (systemic diseases like TB, DM, jaundice, bronchial asthma, cardiovascular diseases, Chronic liver Disease etc.). 6. Patients with Anorectal disease like Haemorrhoids, fistula, fissures or having any history of psychological disorder. 7. Patient having Acute pelvic inflammatory disease. 8. Patient taking any hormonal therapy and history of Hormonal Contraception within 3 months prior to study , patient taking lipid lowering drugs or other drugs affecting Insulin Senstivity or Serum Androgen.

Design outcomes

Primary

MeasureTime frame
Normalization of certain parameters that include- 1)General Body Parameters a)BMI b)Waist Circumference c)Hip Circumference d)Waist Hip Ratio 2)Hormonal levels: A) Serum FSH on day 2 or 3 of menses B) Serum LH on day 2 or 3 of menses C) LH/FSH ratio D) Serum Prolactin E) Serum TSH F) Serum Testosterone G) Serum AMH 3) HOMA-IR 4) USG (Pelvis) Colour Doppler : Ovarian Volume Number and size of Dominant follicle Uterine Artery Resistive index 5) C-reactive protein 6) Lipid Profile 7) Clinical Hyperandrogenism ( modified Ferriman-Gallway score) 8)LFT and RFT Values Timepoint: A total of 4 follow ups at an interval of one month

Secondary

MeasureTime frame
Improvement in the quality of life of PCOS patients pertaining to their physical mental emotional social & behavioural well beingTimepoint: A standard PCOS Questionnaire will be attempted at baseline before the start of treatment & at the end of 3 months that is after the end of treatment

Countries

India

Contacts

Public ContactDr Preeti Chouhan

Institute of Medical sciences Faculty of Ayurveda Banaras Hindu University

drpchouhan1990@gmail.com9413636378

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026