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CTRI Number  CTRI/2026/02/102968 [Registered on: 04/02/2026] Trial Registered Prospectively
Last Modified On: 07/02/2026
Post Graduate Thesis  No 
Type of Trial  Interventional 
Type of Study   Ayurveda 
Study Design  Single Arm Study 
Public Title of Study   To evaluate the efficacy of Vayasthapana Gana Kashayam in the management of menopausal symptoms 
Scientific Title of Study   An Open Label Single Arm Clinical Study To evaluate the efficacy of Vayasthapana Gana Kashayam in the managment of menopausal symptoms in peri menopausal women 
Trial Acronym  NIL 
Secondary IDs if Any  
Secondary ID  Identifier 
NIL  NIL 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Rajalakshmi Ravindran 
Designation  Associate Proffesor and PhD scholar  
Affiliation  Indian Institute of Ayurved Research and Hospital Rajkot 
Address  Depatment of Prasooti Tantra Evam Stree Roga Indian Institute of Ayurved Research and Hospital 150 ft ishwariya road ishwariya post rajkot gujarat
150 ft ishwariya road off kalawad road ishwariya post rajkot 360110
Rajkot
GUJARAT
360110
India 
Phone  09980460845  
Fax    
Email  rajalakshmiravindran@hotmail.com  
 
Details of Contact Person
Scientific Query
 
Name  Rajalakshmi Ravindran 
Designation  Associate Professor and PhD Scholar  
Affiliation  Indian Institute of Ayurved Research and Hospital Rajkot 
Address  Department of Prasooti Tantra Evam Stree Roga Indian Institute of Ayurved Research and Hospital 150 fee ishwariya road off kalawad road ishwariya post rajkot gujarat
150 ft ishwariya road off kalawad road ishwariya post rajkot 360110
Rajkot
GUJARAT
360110
India 
Phone  09980460845  
Fax    
Email  rajalakshmiravindran@hotmail.com  
 
Details of Contact Person
Public Query
 
Name  Rajalakshmi Ravindran 
Designation  Associate Professor and PhD Scholar  
Affiliation  Indian Institute of Ayurved Research and Hospital Rajkot 
Address  Department of Prasooti Tantra Evam Stree Roga Indian Institute of Ayurved Research and Hospital 150 ft. ishwariya road off kalawad road ishwariya post rajkot gujarat
150 ft ishwariya road off kalawad road ishwariya post rajkot 360110
Rajkot
GUJARAT
360110
India 
Phone  09980460845  
Fax    
Email  rajalakshmiravindran@hotmail.com  
 
Source of Monetary or Material Support  
NIL 
 
Primary Sponsor  
Name  Dr Rajalakshmi Ravindran 
Address  Depatment of Prasooti Tantra Evam Stree Roga Indian Institute of Ayurved Research and Hospital 150 ft ishwariya road off kalawad road ishwariya post rajkot gujarat 
Type of Sponsor  Research institution and hospital 
 
Details of Secondary Sponsor  
Name  Address 
NIL  NIL 
 
Countries of Recruitment     India  
Sites of Study  
No of Sites = 1  
Name of Principal Investigator  Name of Site  Site Address  Phone/Fax/Email 
Dr Rajalakshmi Ravindran  Indian Institute of Ayurved Research and Hospital  2nd floor Room no 3 Department of Prasooti Tantra Evam Stree Roga opposite Seminar Hall
Rajkot
GUJARAT 
9980460845

rajalakshmiravindran@hotmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
INSTITUTIONAL ETHICS COMMITTEE OF INDIAN INSTITUTE OF AYURVED RESEARCH AND HOSPITAL  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition:N959||Unspecified menopausal and perimenopausal disorder. Ayurveda Condition: ARTAVAVAHASROTOVIKARAH,  
 
Intervention / Comparator Agent  
snoIntervention/ComparatorTypeDrug-TypeProcedure NameDetails
1Intervention ArmDrugClassical(1) Medicine Name: VAYASTHAPANA GANA KASHAYAM, Reference: CHARAKA SAMHITA SUTRA STHANA ADHYAYA 4, Route: Oral, Dosage Form: Kwatha/ Kashaya, Dose: 50(ml), Frequency: bd, Bhaishajya Kal: Pragbhakta, Duration: 3 Months, anupAna/sahapAna: No, Additional Information: -
 
Inclusion Criteria  
Age From  40.00 Year(s)
Age To  55.00 Year(s)
Gender  Female 
Details  Perimenopausal women fulfilling the diagnostic criteria. STRAW 1 AND 2
MRS total score more or equal to 9 at screening
Menopause rating scale  
 
ExclusionCriteria 
Details  Women with greater than 12 months amenorrhoea
Women with surgical menopause
On Hormonal therapy
Subjects already on drug therapy for the same
Uncontrolled systemic illness
 
 
Method of Generating Random Sequence   Not Applicable 
Method of Concealment   Not Applicable 
Blinding/Masking   Open Label 
Primary Outcome  
Outcome  TimePoints 
To evaluate the efficacy of Vayasthapana Gana kashayam in the management of menopausal symptoms among peri menopausal women.   at baseline and 12 week 
 
Secondary Outcome  
Outcome  TimePoints 
To evaluate the efficacy of Vayasthapana Gana kashayam in improving Quality of life among peri- menopausal women, as assessed by MEN-QOL  at baseline and 12 week 
 
Target Sample Size   Total Sample Size="100"
Sample Size from India="100" 
Final Enrollment numbers achieved (Total)= "Applicable only for Completed/Terminated trials"
Final Enrollment numbers achieved (India)="Applicable only for Completed/Terminated trials" 
Phase of Trial   N/A 
Date of First Enrollment (India)   16/02/2026 
Date of Study Completion (India) Applicable only for Completed/Terminated trials 
Date of First Enrollment (Global)  Date Missing 
Date of Study Completion (Global) Applicable only for Completed/Terminated trials 
Estimated Duration of Trial   Years="1"
Months="0"
Days="0" 
Recruitment Status of Trial (Global)
Modification(s)  
Not Yet Recruiting 
Recruitment Status of Trial (India)  Open to Recruitment 
Publication Details   N/A 
Individual Participant Data (IPD) Sharing Statement

Will individual participant data (IPD) be shared publicly (including data dictionaries)?  

Response - NO
Brief Summary  

INTRODUCTION AND SCOPE

Menopause and the preceding perimenopausal transition are increasingly recognized as significant global health challenges affecting women physical psychological and social well being. According to projections by the World Health Organization by the year 2030 more than one billion women worldwide will be aged fifty years or above experiencing menopause or its transitional phase.

Perimenopause is defined as the transitional period during which a woman body progresses toward menopause culminating in the final menstrual period. The onset of perimenopause is characterized by menstrual irregularities while menopause is confirmed retrospectively after twelve consecutive months of amenorrhea. This transitional phase is associated with progressive decline in ovarian function leading to reduced estrogen and progesterone secretion. Consequently women experience marked hormonal fluctuations that manifest as a wide range of vasomotor psychological urogenital and musculoskeletal symptoms.

The perimenopausal transition has often been described as a biological storm reflecting the complex interplay of endocrine physical and emotional changes that profoundly influence a woman personal familial and social life. Symptoms such as mood disturbances persistent fatigue sleep disorders and altered libido frequently strain marital relationships and interpersonal dynamics. Reduced work efficiency social withdrawal and declining self esteem further compromise overall quality of life.

Conventional management strategies particularly hormone replacement therapy have demonstrated efficacy in alleviating menopausal symptoms. However concerns regarding potential adverse effects and contraindications limit their suitability for all women. This has led to a growing global interest in safe natural and holistic therapeutic alternatives that support women through this physiological transition.

AYURVEDIC PERSPECTIVE

In Ayurveda ageing is described under the concept of Jara one of the Swabhavika Vyadhis denoting a natural and inevitable biological process. Menopause is regarded as a physiological milestone marking the onset of Jara Avastha. Women during this phase are described as Nishphala and Gatartava indicating cessation of fertility and decline in reproductive capacity which heralds the beginning of senescence.

Classical Ayurvedic texts describe Rajonivrutti as occurring around the age of fifty years correlating with the hormonal and reproductive decline recognized in modern physiology. Menopause is thus viewed as a natural transition from a Pitta dominant to a Vata dominant stage of life. The predominance of Vata Dosha in later years contributes to Dhatu Kshaya Sosha dryness reduced vitality and functional instability.

Madhava Nidana describes Jarasosha as a degenerative condition characterized by Vata Prakopa and Dhatu Kshaya leading to depletion of Bala Varna and Ojas. Clinical manifestations such as fatigue dryness of tissues reduced strength and emotional instability closely resemble the symptomatology observed during menopause.

RATIONALE OF THE STUDY

In this context Vayasthapana Gana one of the Rasayana Ganas described by Acharya Charaka holds special therapeutic relevance. It comprises ten medicinal plants Amalaki Phyllanthus emblica Haritaki Terminalia chebula Guduchi Tinospora cordifolia Rasna Pluchea lanceolata Aparajita Clitoria ternatea Punarnava Boerhavia diffusa Jeevanti Leptadenia reticulata Shatavari Asparagus racemosus Mandukaparni Centella asiatica and Sthira Desmodium gangeticum.

These drugs possess proven antioxidant Rasayana Vatashamaka and Dhatuvardhaka properties supported by various in vitro and in vivo studies. The term Vayasthapana literally denotes that which sustains youthfulness emphasizing preservation of tissue integrity vitality and functional balance.

Preliminary studies on Vayasthapana Gana have demonstrated promising outcomes in reducing menopausal symptoms and improving overall well being. However robust clinical evidence remains limited.

Therefore the present study is designed to evaluate the efficacy of Vayasthapana Gana Kashayam in the management of menopausal symptoms and enhancement of quality of life among perimenopausal women. This intervention may offer a safe natural and holistic alternative to conventional therapies supporting physical equilibrium emotional stability and overall health during this pivotal stage of life.

OBJECTIVES

Primary Objective
To evaluate the efficacy of Vayasthapana Gana Kashayam in the management of menopausal symptoms among perimenopausal women.

Secondary Objective
To evaluate the efficacy of Vayasthapana Gana Kashayam in improving quality of life among perimenopausal women assessed using MENQOL questionnaire.

HYPOTHESES

Null Hypothesis
Vayasthapana Gana Kashayam has no significant effect on reducing menopausal symptoms or improving quality of life.

Alternate Hypothesis
Vayasthapana Gana Kashayam significantly reduces menopausal symptoms and improves quality of life.

STATEMENT OF THE RESEARCH PROBLEM

Menopause and the perimenopausal transition represent a growing global health burden with millions of women experiencing distressing vasomotor psychological urogenital and musculoskeletal symptoms that markedly impair quality of life. Although conventional therapies such as hormone replacement therapy are effective their associated risks and contraindications necessitate the exploration of safer and holistic alternatives. From an Ayurvedic perspective menopause corresponds to Jara Avastha characterized by Vata predominance and Dhatu Kshaya. Despite the therapeutic potential of Vayasthapana Gana clinical evidence validating its efficacy remains limited. Hence the present study aims to scientifically evaluate the effectiveness of Vayasthapana Gana Kashayam in managing menopausal symptoms and improving quality of life in perimenopausal women.

REVIEW OF LITERATURE

Disease Review
A comprehensive review of perimenopause menopause menopausal symptoms and the Ayurvedic concept of Rajonivrutti will be undertaken using classical Ayurvedic texts contemporary medical literature research articles and standard textbooks.

Drug Review
A detailed review of Vayasthapana Gana will be conducted.

PHARMACEUTICAL STUDY

The study drug will be prepared at the Pharmacy of Indian Institute of Ayurved and Research Hospital Rajkot following Standard Operating Procedures. The Kashayam will be prepared according to Kwatha Kalpana guidelines as per the Ayurvedic Formulary of India. Raw drugs will be identified and authenticated using pharmacognostical parameters. A preliminary pharmaceutical study will be undertaken for preparation and standardization of the formulation.

MATERIALS AND METHODS

Study Design
Open label single arm clinical study with pre and post treatment evaluation.

Sample Size
Minimum of one hundred participants fulfilling inclusion and diagnostic criteria.

Study Setting
Perimenopausal women attending the PTSR outpatient department of Indian Institute of Ayurved Research Hospital Rajkot and Glocal Ayurveda Medical College Mirzapur Pole Saharanpur Uttar Pradesh.

TREATMENT PROTOCOL

Drug Vayasthapana Gana Kashayam
Dose fifty milliliters twice daily
Time before food
Route oral
Duration three months twelve weeks

INFORMED CONSENT

Written informed consent will be obtained from all participants in accordance with World Health Organization Research Ethics Review Committee guidelines. The consent document will include a patient information sheet and certificate of consent.

DIAGNOSTIC CRITERIA

Diagnosis of perimenopause will be based on STRAW staging menstrual based reproductive stage.

Early menopausal transition Persistent difference of seven days or more in cycle length
Late menopausal transition Amenorrhea of more than sixty days but less than twelve months

INCLUSION CRITERIA

Women aged forty to fifty five years
Perimenopausal women fulfilling STRAW diagnostic criteria
Menopause Rating Scale score nine or more at screening

EXCLUSION CRITERIA

Women with amenorrhea more than twelve months
Women with surgical menopause
Women on hormonal therapy
Subjects already on treatment for menopausal symptoms
Uncontrolled systemic illness

ASSESSMENT CRITERIA

The study will utilize Menopause Rating Scale questionnaire for assessment of menopausal symptoms. Overall efficacy will be assessed based on reduction in total Menopause Rating Scale score. Quality of life will be assessed using MENQOL questionnaire at baseline and after treatment.

CRITERIA FOR OVERALL ASSESSMENT OF THERAPY

Marked improvement More than seventy five percent relief
Moderate improvement Fifty to seventy five percent relief
Mild improvement Less than fifty percent relief
Unchanged Less than twenty five percent relief

TIME POINTS

Assessment will be carried out at baseline and after completion of twelve weeks of treatment.

WITHDRAWAL CRITERIA

Subjects developing serious adverse events poor compliance or loss to follow up will be withdrawn from the study and referred to appropriate care centers.

STATISTICAL ANALYSIS

The collected data will be analyzed using descriptive statistics Student t test and other appropriate statistical methods

 
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