Effect of Mansyadi Ghanvati and night regimen with or without Bhramari Pranayama in disturbed sleep in geriatric population

Efficacy of Mansyadi Ghanvati and Ratricharya with or without Bhramari Kumbhaka in the Management of Mild and Short-term Insomnia in Geriatric Population - An Open Labelled Randomized Comparative Clinical Trial - NIL

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/03/083018

Enrollment

Registered

2025-03-21

Start date

Unknown

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

Health Condition 1: G470- Insomnia

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1 Age group - 60-80 years 2 Patients of mild and short-term insomnia. 3 Patients willing to accept the participation in clinical trial. 4 Individuals with controlled primary systemic diseases.

Exclusion criteria

Exclusion criteria: 1 Age below 60 years and above 80 years. 2 Patients suffering from chronic insomnia disorder. 3 Patients suffering from severe or moderate insomnia. 4 Secondary Insomnia. 5 Fatal Familial Insomnia. 6 Patients with alcohol or drug dependency. 7 Advanced chronic illnesses such as bronchial asthma, diabetes, cancer, liver cirrhosis, chronic renal failure. 8 Acute illnesses such as cerebrovascular accidents, myocardial infarction, COPD, epilepsy. 9 uncontrolled systemic diseases like Diabetes (Random Blood sugar not more than 200 mg/dl), hypertension (not more than 180/100 mm Hg). 10 Patients with major psychiatric illnesses like schizophrenia, depressive psychosis, bipolar disorders, obsessive compulsive disorder, personality disorders, mood disorders, panic disorders, post-traumatic stress disorders.

Design outcomes

Primary

Measure	Time frame
Improvement in quality of sleep of the patients with mild and short Insomnia in geriatric population according to ICSD criteria.Timepoint: 8 weeks	—

Secondary

Measure	Time frame
Improvement in associated complains of Anidra. Improvement in the level of stress. Timepoint: 8 weeks	—

Countries

India

Contacts

Public ContactProf Arpan A Bhatt

Institute of Teaching and Research in Ayurveda

vdarpansoniac@itra.edu.in9998968727

Outcome results