Study of effect of panchendriyavardhan tail on sleep in patients suffering from sleeplessness

An open label prospective phase II clinical study to evaluate efficacy and safety of panchendriyavardhan tail in the insomnia

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2018/03/012679

Enrollment

Registered

2018-03-20

Start date

Unknown

Completion date

Unknown

Last updated

2021-11-24

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

Conditions

None listed

Interventions

Intervention1: Panchendriyavardhan tail: 5 drops Nasya procedure at bed time for 30 days in each nostril Control Intervention1: NIL: NIL

Eligibility

Inclusion criteria

Inclusion criteria: Healthy volunteers suffering from insomnia and willing to give written informed consent

Exclusion criteria

Exclusion criteria: Volunteers with chronic illness

Design outcomes

Primary

Measure	Time frame
To study the efficacy of Panchendriyavardhan tail on total sleep time To study the efficacy of Panchendriyavardhan tail nasyaon change in the WASO (wake time after sleep onset)Timepoint: 30 days	—

Secondary

Measure	Time frame
To study the efficacy of Panchendriyavardhan tail average sleep latency per night from baseline To study the efficacy of Panchendriyavardhan tail hamilton anxiety scale at baseline week 1 and week 2 To study the efficacy of Panchendriyavardhan tail average number of night time awakening per night from baseline week 1 and week 2Timepoint: 30 days	—

Countries

India

Contacts

Public ContactDr Savita Kulkarni

Maharashtra University of Health Sciences Nashik

drsavita.k07@gmail.com2532517170

Outcome results