Clinical trial of shatavari churna in premenstrual syndrome

A SINGLE ARM CLINICAL STUDY OF SHATAVARI CHURNA IN PITTAVRITTA VYANA VAYU W.S.R.TO PREMENSTRUAL SYNDROME

Status

Active, not recruiting

Phases

Phase 1Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2022/04/042193

Enrollment

100

Registered

2022-04-27

Start date

Unknown

Completion date

Unknown

Last updated

2022-05-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: N943- Premenstrual tension syndrome

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patient fullfilling criteria of pitta avritta vyana vayu 2.Regular menstruating women & whose periodic cycle is regular 2-6 days(25-31 Days cycle) 3.Patient irrespective of marital status,obstretic status.education,occupationa

Exclusion criteria

Exclusion criteria: 1.K/H/O mood disturbance because of any systemic disorder/any otherpsychiatric disorders 2.Women with K/H/O severe systemic illness 3.Women who taking oral contraceptive & hormone replacement therapy 4.Premature ovarian failure 5.Major gynaecological disorders

Design outcomes

Primary

Measure	Time frame
To decrease the symptoms of Pitta Avrutta Vyana Vayu w.s.r to Premenstrual Syndrome on assessment of subjective parameters like Sarvanga Daha,Klama,Gatra Vikshepa Sanga, Santana,VedanaTimepoint: 3 months	—

Secondary

Measure	Time frame
1.To reduce the signs & symptoms 2.To assess improvement by parameters VAS. 3.To study the etio-pathology of Pitta avrutta vyana vayu & premenstrual disorder in detail with classic ayurved & modern text 4.To achieve the out-come of study in 120 days. Timepoint: 120 Days	—

Countries

India

Contacts

Public ContactSagar Dherange

Yashwant Ayurved College

dr.chodankarsmita@gmail.com08329279770

Outcome results