A clinical trial on Ayurvedic formulation in the management of VatikaArtavadushti w.s.r. to Menstrual Disorder.

Phase 2

• Conditions: Health Condition 1: N948- Other specified conditions associated with female genital organs and menstrual cycle

• Registration Number: CTRI/2022/05/042352
• Lead Sponsor: ATIONAL INSTITUTE OF AYURVEDA

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 30 May 2022

Recruitment & Eligibility

• Status: ot Yet Recruiting
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

Patients complaining of Vatika Artavadushti with any two of the following manifestations:

1. Artava vaivarnya (Discolored Menstrual Blood) - Aruna varna (Red/Reddish Brown/Tawny) or Shyava varna (Dark Brown) or Krishna varna (Black).

2. Alpa Artava (Hypomenorrhoea)

3. Vicchinna Artava (Interrupted flow)

4. Saruja Artava (Painful Menses)

5. Artava Chiraat Nishichyate (Oligomenorrhoea).

Female patients of age group 12 â?? 50 years.

Hb% >= 8 gm/dl.

Exclusion Criteria

1. Pregnant woman

2. Patient having any systemic disease.

3. Post menopausal woman.

4. Patient having any type of malignancy.

5. Patient having Sexually Transmitted Diseases.

6. Patient using oral contraceptive pills and Intra Uterine Contraceptive

Devices.

7. Patient with thyroid hormone abnormalities.

8. Patient having any other Uterine or Pelvic pathology like â?? Polyp,

Endometrial Tuberculosis, Fibroid, Adenomyosis, Pelvic

Inflammatory Diseases, etc.

9. Patients vaccinated for COVID-19 within three months.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Achievement of normal menstruation. <br/ ><br>Timepoint: 2 MONTHS <br/ ><br>

Secondary Outcome Measures

Name	Time	Method
Improvement in quality of life.Timepoint: 2 MONTHS