Clinical study to evaluate the efficacy of panchvalkaladi taila yoni pichu in the management of paripluta yonivyapad

A clinical study to evaluate the efficacy of panchvalkaladi taila yoni pichu in the management of paripluta yonivyapad - nil

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/05/086906

Enrollment

Registered

2025-05-14

Start date

Unknown

Completion date

Unknown

Last updated

2025-05-26

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

Conditions

Health Condition 1: N739- Female pelvic inflammatory disease, unspecified

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Married women within the age group of 18-45yeras diagnosed with paripluta yonivyapad with complains of shotha in yoni or vedna in shroni or vankshana or kati with vaginal discharge

Exclusion criteria

Exclusion criteria: Pregnant women or reproductive malignancy or prolapse uterus or patient suffering from major systematic disorders

Design outcomes

Primary

Measure	Time frame
Primary outcome from this study will be effective for the patient in the management of paripluta yonivyapad with Allopathic medication can treat the disease faster but the recurrence chances is higher because allopathic medicine only works on symptoms of the disease in contrast ayurvedic treatment works on principal of hetu dosh kal prakritiTimepoint: Primary outcome from this study will be seen after 7 days of Pradhan karma and after follow up of 15 days	—

Measure

Time frame

Primary outcome from this study will be effective for the patient in the management of paripluta yonivyapad with Allopathic medication can treat the disease faster but the recurrence chances is higher because allopathic medicine only works on symptoms of the disease in contrast ayurvedic treatment works on principal of hetu dosh kal prakritiTimepoint: Primary outcome from this study will be seen after 7 days of Pradhan karma and after follow up of 15 days

—

Secondary

Measure	Time frame
Secondary outcome from this clinical study could be used for making line of treatment for paripluta yonivyapad & Also it could be used by health ministery as a Health scheme for the management of paripluta yonivyapadTimepoint: Secondary outcome will be assessed after 5months of research process on this study	—

Countries

India

Contacts

Public ContactDr Trilochan Mohanto

Sri sai ayurvedic pg medical college and hospital

tmahanta72@gmail.com9993304678

Outcome results