The Single Arm Clinical Study To Evaluate The Effect Of Hingvadi Gutika In Udavarta Yonivyapada

Phase 2

Not yet recruiting

• Conditions: Primary dysmenorrhea. Ayurveda Condition: YONIROGAH/YONI-VYAPADAH,

• Registration Number: CTRI/2024/01/061928
• Lead Sponsor: SANE GURUJI AROGYA KENDRA

Brief Summary

THIS IS AN OPEN LABEL SINGLE ARM  CLINICAL STUDY TO EVALUATE THE EFFECT OF HINGVADI GUTIKA IN UDAVARTA YONIVYAPADA.

THE PRIMARY OBJECTIVE IS TO STUDY THE EFFECT OF HINGVADI GUTIKA IN UDAVARTA YONIVYAPADA FOR A DURATION OF 60 DAYS.

REGULAR ASSESSMENT OF SIGNS AND SYMPTOMS WILL BE DONE. OBSERVATION WILL BE DRAWN FROM THE OUTCOME OF PATIENT.

Detailed Description

Not available

Study Timeline

• Last Update Posted: 2024-01-28
• Study Start: 2024-02-15

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: Female
• Target Recruitment: 30

Inclusion Criteria

• Patient suffering from udavarta Yoni Vyapada 2.
• Married or unmarried patient of age group 20 to30 yrs 3.
• Patient having pain during Menstruation 4.
• Patient having painful menses as compared to previous menses 5.
• Patient ready for clinical trial.

Exclusion Criteria

• Hypothyroidism, HIV, HbsAg, VDRL, prolactaemia, tuberculosis,utrine fibroid,complex ovarian cyst, dermoid cyst, tubo-ovarian mass, cervical polyp or growth.
• 5 Patients suffering from uterine synechiae, endometriosis or malignancy.
• 6 Pregnancy lactating and post natal female.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The effect of Hingvadi Gutika 250 mg BD orally in Udavarta Yonivyapada	18 months

Secondary Outcome Measures

Name	Time	Method
Literature study of Udavarta Yonivyapada.	Preparation of Hingvadi Gutika

Trial Locations

Locations (1)

Sane Guruji Arogya Kendra; 🇮🇳 Pune, MAHARASHTRA, India

Sane Guruji Arogya Kendra

🇮🇳Pune, MAHARASHTRA, India

Dr Prachi Sanjog Pardeshi

Principal investigator

8999822065

pardeshiprachie30@gmail.com