A Clinical Study Comparing the Effect of Krishnatil Kashaya with Kinshuka Kshara and Murchita Til Tail Matra Basti in Participants of Udavarta Yonivyapad Primary Dysmenorrhea An Intervention-Based Analysis

A COMPARATIVE CLINICAL ANALYSIS OF KRISHNATIL KASHAYA WITH KINSHUKA KSHARA AND MURCHITA TIL TAIL MATRA BASTI IN UDAVARTA YONIVYAPAD WITH SPECIAL REFERENCE TO PRIMARY DYSMENORRHEA - NIL

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/07/091191

Enrollment

Registered

2025-07-18

Start date

Unknown

Completion date

Unknown

Last updated

2025-07-21

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

Conditions

Health Condition 1: N944- Primary dysmenorrhea Health Condition 2: N944- Primary dysmenorrhea

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Patient with painful menstruation without any pelvic pathology. Age group of 14-30 years. Pain associated scanty amount of blood flow. Patient willing to participate in the study by signing written consent.

Exclusion criteria

Exclusion criteria: Dysmenorrhea with pelvic pathology. Patients who need surgical intervention. Patient with any systemic illness.

Design outcomes

Primary

Measure	Time frame
It is expected that at the end of the study will be able to demonstrate the effect of Til kashaya with kinshuka kshara in the management of udavarta yonivyapad.Timepoint: Evaluation after one month	—

Secondary

Measure	Time frame
Reduction in severity of pain Reduction in duration pf pain Reduction in artavasrava awadhi Reduction in quantity of blood loss Reduction in radiation of pain Reduction in interval of cycle Reduction in praseka Reduction in chhardi Reduction in atisara Reduction in shrama Reduction in shirashula Reduction in giddiness Reduction in constipation Reduction in anorexia Timepoint: Evaluation after 1 month	—

Measure

Time frame

Reduction in severity of pain Reduction in duration pf pain Reduction in artavasrava awadhi Reduction in quantity of blood loss Reduction in radiation of pain Reduction in interval of cycle Reduction in praseka Reduction in chhardi Reduction in atisara Reduction in shrama Reduction in shirashula Reduction in giddiness Reduction in constipation Reduction in anorexia Timepoint: Evaluation after 1 month

—

Countries

India

Contacts

Public ContactDrBasanti Guru

Pandit Khushilal Sharma Government (Autonomous)Ayurveda College and Institute Bhopal MP

basantiayu75@gmail.com09827579276

Outcome results