Exploring the role of Lasunadaya Ghrita pana and nasya in primary depression:A non randomized open clinical study.

Phase 2

Completed

• Conditions: Health Condition 1: F321- Major depressive disorder, singleepisode, moderateHealth Condition 2: null- primary depression

• Registration Number: CTRI/2019/08/020756
• Lead Sponsor: Self

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2019-05-06
• Last Update Posted: 24 November 2021

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 56

Inclusion Criteria

Patient diagnosed as primary depression as per ICD-10 criteria.patient having depression for not more than two years.patients willing to participate in the study voluntarily giving their informed consent.patient not having any other physical and mental co-morbidity considered as contraindication to the treatment.

Exclusion Criteria

Patient below 20 years and over 60 years.Patients having any other psychiatric co-morbidity.Patient having cognitive malfunctions due to substance abuse or due to age related dementia or mental retardation.Females in the stage of pregnancy or lactation.Patients having suicidal ideation or history of attempted suicide.Patients with marked irritable,unstable and violent behaviour.Patients allergic to any component of medication.Patients unable to take lasun or go-mutra due to their personal customs or belief.Patients not giving the consent for the study.Any condition where nasya is contraindicated.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Improvement in Hamilton Depression ScaleTimepoint: Base line and 4 week

Secondary Outcome Measures

Name	Time	Method
SF-36Timepoint: Base line and Week 4