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Clinical trial of Dashmoola Vati and Sahacharadi Vati in Sutika Shoola

A Comparative Clinical Study To Evaluate The Efficacy Of Dashmoola Vati And Sahcharadi Vati In Sutika Shoola - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/01/100936
Enrollment
60
Registered
2026-01-13
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Health Condition 1: O908- Other complications of the puerperium, not elsewhere classified Health Condition 2: O908- Other complications of the puerperium, not elsewhere classified

Interventions

None listed

Sponsors

Dr Shubham Ramnath Karle
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patient with Full Term Normal Delivery with Sutika-shool will be selected. Patients from age-group 19 to 40 years of age will be selected. Patients of any parity will be included

Exclusion criteria

Exclusion criteria: Retained placental bits Uterine rupture Post-Partum Haemorrhage (Primary and secondary) Haematoma at episiotomy/Perineal region Forcep delivery Ventose delivery Patient with Tubo-ovarian Mass, Twisted ovaryPatient with known uterine anomaly, Fibroid, etc Patient with manual removal of Placenta Patient with known systemic disease, i.e. Diabetes, Renal/Cardiac disease, severe anaemia, GDM, Immuno-compromised patients etc. Caesarean Section Puerperal Tubal Ligation Sutika taking snehan, swedan and doopan

Design outcomes

Primary

MeasureTime frame
To evalute the efficacy of Dashmoola vati and sahcharadi vati in sutika shoola in duration of 7 daysTimepoint: To evalute the efficacy of Dashmoola vati and sahcharadi vati in sutika shoola in duration of 7 days

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactDr Kalpana Bajrang Ayare

MAM S Sumatibhai Shah Ayurved Mahavidyalaya Malwadi Hadapsar Pune

drkalpanaayare@gmail.com9423295630

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026