Skip to content

THE COMPREHENSIVE APPROACH A CLINICAL STUDY TO EVALUATE EFFICACY OF COMBINING VIDDHA KARMA AND NASYA KARMA IN OVULATION INDUCTION.

A RANDOMIZED CONTROLLED TRIAL TO EVALUATE THE COMBINED EFFECT OF VIDDHA KARMA AND LAKSHMANA SIDDHA GHRITA NASYA KARMA IN OVULATION INDUCTION - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/02/104046
Enrollment
40
Registered
2026-02-16
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: N970- Female infertility associated withanovulation

Interventions

None listed

Sponsors

Dr Simaran Verma
Lead Sponsor
Dr Swathi C
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patient diagnosed with primary and secondary infertility due to anovulation. 2. Patient with age group between 20-40 years with anovulatory cycle. 3. Patient eligible for Viddhakarma. 4. Patient eligible for Nasya. 5. Patient, who is willing to participate in the study.

Exclusion criteria

Exclusion criteria: 1. Female patient having age less than 20 years and more than 40 years. 2. Sexually transmitted disease ( HIV, HBsAg ,VDRL, Anti HCV)

Design outcomes

Primary

MeasureTime frame
The ovulation rate, defined as the proportion of women achieving confirmed ovulation during the intervention cycle, assessed by serial transvaginal ultrasonography(follicular scan)Timepoint: 7 days

Secondary

MeasureTime frame
1.To assess the change in dominant follicular size measured by serial transvaginal ultrasonography. 2.To evaluate endometrial thickness at the time of ovulation. 3.To evaluate the endometrial pattern at the time of ovulationTimepoint: 7 days

Countries

India

Contacts

Public ContactDr Simaran Verma

Sri Jayendra Saraswathi Ayurveda College and Hospital, Chennai, Tamil Nadu 600123, India

drswathi@sjsach.org.in81057754944

Outcome results

None listed

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