MedPath

A clinical study to evaluate the efficacy of Kalajaji taila orally in Artava kshaya, Oligohypomenorrhea for a period of 3 consecutive menstrual cycles

Phase 2
Conditions
Health Condition 1: N915- Oligomenorrhea, unspecified
Registration Number
CTRI/2024/07/069778
Lead Sponsor
Dr Pratheeksha M
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1. PATIENTS WILLING TO BE PART OF TREATMENT OF ARTAVAKSHAYA, OLIGOHYPOMENORRHEA.

2. PATIENTS FULFILLING THE CARDINAL SYMPTOMS OF ARTAVAKSHAYA, OLIGOHYPOMENORRHEA.

3. WOMEN OF AGE GROUP 18- 40 YEARS.

Exclusion Criteria

1. MARKED ANEMIA (HB LESSER THAN 7G).

2. SUBJECTS ON ORAL CONTRACEPTIVE PILLS, INTRA UTERINE CONTRACEPTIVE DEVICES.

3. SUBJECTS SUFFERING FROM ANY SYSTEMIC ILLNESS SUCH AS HYPERTENSION AND DIABETES MELLITUS.

4. LACTATING WOMEN.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
© Copyright 2025. All Rights Reserved by MedPath