A clinical study to assess the effect of Guduchi Ghanavati in women suffering from premenstrual syndrome (PMS)

Randomised open controlled clinical study to evaluate the efficacy of Guduchi Ghanavati in Pittavritta Vyana Vayu w.s.r. to Premenstrual syndrome - NIL

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2026/02/103888

Enrollment

136

Registered

2026-02-16

Start date

Unknown

Completion date

Unknown

Last updated

2026-03-02

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 fulfilling diagnostic criteria of pitsavita vyana vayu based on symptoms 2. Patients are selected of age group between 15-40 years 3. Regular menstruating females and whose periodic cycle is regular 2-6 days (25- 31day cycle) 4. patient irrespective of marital status, education, occupation 5. patient irrespective of caste and socioeconomic status

Exclusion criteria

Exclusion criteria: 1. Known history of severe mood disturbance because of any systemic disorder/any other psychiatric disorders& patient on antipsychotic drugs 2. Women with known history of severe systemic illness 3. Women who taking oral contraceptives and hormone replacement therapy 4. Known case of Diabetes/Hypertension 5. Known case of Hypothyroidism 6. pregnant females 7. Major gynaecological disorders (Endometriosis, PID, perimenopause)

Design outcomes

Primary

Measure	Time frame
To evaluate the efficasy of guduchi ghanavati in pittavritta vyan vayu w.s.r to premenstrual syndromeTimepoint: 3 months	—

Secondary

Measure	Time frame
1.To reduce the symptoms of pittavritta vyana vayu lakshanas W.S.R to symptoms of premenstrual syndrome. 2. to assess improvement by gradation of PMS symtoms scale(sarvangdaha , klama , gatra vikshepa , sanga ,constipation ,santapa,vedna, bloating) 3. To study the etiopathology of pittavritta vyan vayu and premenstrual disorderd in detail with classic ayurveda and modern text along with published dada . 4.To achieve the outcome of study in 90 days.Timepoint: 90 days	—

Measure

Time frame

1.To reduce the symptoms of pittavritta vyana vayu lakshanas W.S.R to symptoms of premenstrual syndrome. 2. to assess improvement by gradation of PMS symtoms scale(sarvangdaha , klama , gatra vikshepa , sanga ,constipation ,santapa,vedna, bloating) 3. To study the etiopathology of pittavritta vyan vayu and premenstrual disorderd in detail with classic ayurveda and modern text along with published dada . 4.To achieve the outcome of study in 90 days.Timepoint: 90 days

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Countries

India

Contacts

Public ContactDr Sandhya Ashokrao Bhujbal

Yashwant ayurvedic college postgraduate training and research centre

vishalaturlapati@gmail.com9960217429

Outcome results