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To evaluate efficacy of Traditional Ayurvedic Formulation (Divya Santati Sudha) in female infertility.

To evaluate efficacy of Traditional Ayurvedic Formulation (Divya Santati Sudha) in female infertility: an observational, single-arm, prospective study.

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/08/056245
Enrollment
69
Registered
2023-08-08
Start date
Unknown
Completion date
Unknown
Last updated
2023-08-21

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

Conditions

Health Condition 1: N979- Female infertility, unspecified

Interventions

None listed

Sponsors

Patanjali Research Institute governed by Patanjali Research Foundation Trust
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Clinically diagnosed with Primary or secondary infertility. 2. Availability and willingness to provide consent.

Exclusion criteria

Exclusion criteria: 1. Patient known to have any Malignancies, chronic Hyper/hypothyroidism. 2. Patient diagnosed with congenital uterine defects. 3. Male partner with abnormal seminal analysis and unwillingness to get treated. 4. Participant habituated to alcohol consumption, smoking or any other substance abuse. 5. The subjects not willing to provide consent.

Design outcomes

Primary

MeasureTime frame
To assess the quality of the life and problem related infertility of the subject by the help of Fertility quality of life (FertiQoL) and The fertility problem inventory.Timepoint: Baseline, 30 day, 60 day and 90 day.

Secondary

MeasureTime frame
To assess the quality of the life and problem related infertility of the subject by the help of Fertility quality of life (FertiQoL) and The fertility problem inventory.Timepoint: Baseline, 30 day, 60 day and 90 day.

Countries

India

Contacts

Public ContactDr Devika Balagopalan

Patanjali Research Institute

drvika.balagopalan@patanjali.res.in7293549081

Outcome results

None listed

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