MedPath

To study the effect of two Ayurveda medicines in patients with excessive menstrual bleeding

Phase 2
Conditions
Health Condition 1: null- Dysfunctional uterine bleeding
Registration Number
CTRI/2018/04/013081
Lead Sponsor
ational institute of Ayurveda
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Closed to Recruitment of Participants
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Patients complaining of Asrigdara as a cardinal symptom.

1.Heavy menstrual bleeding (amount >80ml) or

2.Prolonged menstrual bleeding (duration >7 days) or

3.Inter menstrual bleeding or

4.Frequent menstrual cycle (interval < 21 days)

Exclusion Criteria

1.Pregnant women.

2.Patients having bleeding due to abortion.

3.Patients having bleeding after menopause.

4.Patients having coagulation disorders.

5.Any type of malignancy.

6.Patients having STIs.

7.Patients having systemic diseases.

8.Patients having bleeding due to uterine or pelvic pathology

9.Patients using IUCD.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Improvement in symptoms and signs of dysfunctional uterine bleedingTimepoint: 3 months
Secondary Outcome Measures
NameTimeMethod
Restoration of normal menstrual cycle i.e amount and intervalTimepoint: 6 months
© Copyright 2025. All Rights Reserved by MedPath