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Use of Kusadi(Darbha)Taila Uttar Basti in the Management of Vandhyatva (Anovulation)

Clinical study to evaluate the efficacy of Kusadhya Taila Uttar Basti in the Management of Vandhyatva w.s.r to Anovulation - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/04/109083
Enrollment
40
Registered
2026-04-22
Start date
Unknown
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

Health Condition 1: N970- Female infertility associated withanovulation

Interventions

None listed

Sponsors

Dr Anshika Goel
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All cases of primary or secondary infertility confirmed with anovulation on folliculometry Married Female patients of the age group 21 to 35 years One fallopian tube must be patent Male counterpart should be normal in all aspects Patients willing to participate in this trial through written informed consent

Exclusion criteria

Exclusion criteria: Congenital anatomical defects of reproductive tract like Bicornuate uterus etc Pathologies as Cervical Stenosis,Malignancy etc Infertility due to peritoneal factors,uterine factors and cervical factors Patient suffering from diseases such as Diabetes Mellitus,Hypertension ,Hypothyroidism, Hyperthyroidism,Tuberculosis,Renal disorder etc Patient taking Hormonal therapy from last 3 months or any other treatment Bilateral tubal blockage Infertility due to abnormality in male partner

Design outcomes

Primary

MeasureTime frame
Follicles getting rupture as seen in USGTimepoint: 3 months The drug trial will be given for 3 days for 3 consecutive menstrual cycle after the cessation of menses

Secondary

MeasureTime frame
Improvement in menstrual cycle parameters Dominant follicle size Endometrial thickness Conception rateTimepoint: After analyzing all the parameters the result will be assessed on the basis of symptomatic relief and improvement. Partially improvement After 1 month-patient get 40-60 percent relief from sign and symptoms Improvement After 2 month patient get 60-80 percent relief from sign and symptoms Cured after 3 months-patient get 80-100 percent relief from sign and symptoms.

Countries

India

Contacts

Public ContactDr Bhappil Sharma

Vaidya Yagya Dutt Sharma Ayurved Mahavidyalaya Khurja

drbhapilsharma@gmail.com7018687930

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: May 1, 2026