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comparative study of shatapushpa taila nasya & shatapushpa churna in artavakshya

Not Applicable
Conditions
Health Condition 1: E663- OverweightHealth Condition 2: E282- Polycystic ovarian syndrome
Registration Number
CTRI/2023/07/055258
Lead Sponsor
Dr Lalita Prajapat
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

Age group 18- 40 yrs.

Interval between two menstrual cycles is greater than 35 days. (for the last 6 months approximately)

The duration of menstrual flow is 2 days or less. .(for the last 6 months approximately)

The quantity of menses is less than 20 ml.

Poly Cystic Ovarian Disease (PCOD) with the symptom of oligomenorrhea and hypomenorrhea.

Exclusion Criteria

Patients below the age of 18 years and above the age of 40 years.

Positive history of venereal diseases (HIV, HBsAg, Anti HCV, VDRL, HPV, Genital herpes, etc.)

Pregnant women, lactating mothers.

Poly Cystic Ovarian Disease (PCOD) with menorrhagia.

Patient having organic pathology of uterus & adnexa like cervical carcinoma or any malignant growth.

Patients will not give consent to participate in the study.

Patients using oral contraceptive pills.

Patients who cannot attend follow-up regularly. Who is participating in another study.

Women suffering from Nasal polyp, D.N.S.(Deviated nasal septum), Rhinitis. Nasal tumor, and history of nasal surgery previous.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Regular Menstrual Cycle Improvement of quality of life <br/ ><br>Timepoint: Every 4weeks
Secondary Outcome Measures
NameTimeMethod
1.Interval between two cycles (intermenstrual period/Duration between two Artava darshana) <br/ ><br>2.Amount of menstrual flow (Artava strava pramana ) <br/ ><br>3.Pain during menses (Yoni vedana) <br/ ><br>Quality of life <br/ ><br>Timepoint: 90days
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