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Effect of Uttar Basti and Pratimarsh Nasya with Shatpushpa Tail in the management of Stree Bandhyattava w.s.r. to Tubal Blockage and Anovulation.

"A clinical study to evaluate the efficacy of Uttar Basti and Pratimarsh Nasya with Shatpushpa Tail in the management of Stree Bandhyattava w.s.r. to Tubal Blockage and Anovulation."

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/09/045753
Enrollment
30
Registered
2022-09-21
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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 Health Condition 2: N971- Female infertility of tubal origin

Interventions

None listed

Sponsors

State Ayurvedic College and Hospital Lucknow
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) Age between 20 to 40 years 2) Patient coming with primary and secondary infertility 3) Patient coming with unilateral/ bilateral/ partial tubal blockage 4) Patient coming with complaints of Ovulatory Dysfunction as per follicular study

Exclusion criteria

Exclusion criteria: 1) Age below 20 and above 42 years 2) Patient coming with menstrual disorders like- menorrhagia, menometrorrhagia, secondary amenorrhoea of more than three months 3) Patient coming with acute inflammatory/ infectious state of genital organs like- PID, Endometriosis, genital tuberculosis, genital prolapse etc. 4) Patient coming with complaints of infertility with cervical/ vaginal/ unknown factor 5) Any congenital anomalies of genital organ 6) Patient suffering with any Systemic/ Acute illness 7) Any significant abnormality found in Husbands seminogram

Design outcomes

Primary

MeasureTime frame
To assess the efficacy of trial therapy on subjective criteria like abnormalities in menstrual cycle - duration, interval, amount of bleeding , pain, and other associated symptom like stress and insomnia. And on Objective criteria- Conception , Tubal patency, Ovulation, Endometrial thickness.Timepoint: Final assessment will be done after completion of trial of 6 Months.

Secondary

MeasureTime frame
Secondary outcome will be done on the basis of changes seen in subjective and objective criteriaTimepoint: six months

Countries

India

Contacts

Public ContactDr Shikha Sharma

State Ayurvedic College and Hospital Lucknow UP

drshikhasharma1982@gmail.com8743976379

Outcome results

None listed

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