Assessment of qulity of life of cancer patient after receving Bio-bliss sryup

Phase 2

Completed

• Conditions: Health Condition 1: D499- Neoplasm of unspecified behavior of unspecified site

• Registration Number: CTRI/2024/02/063254
• Lead Sponsor: A for Ayurveda

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Completion: 2024-07-05
• Last Update Posted: 22 July 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 26

Inclusion Criteria

Patients of both gender aged 18-70 years

dignosed patients of cancer of any origin in general

patients who had on going or not taking any treatment like chemotherapy and or radiation therapy

Exclusion Criteria

patients who are not willing to participate in the study

severely ill with many complication

Any other condition which may jeopardize the study

Any other condition in which the investigators opinion would preclude the subject from the participating

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
to evaluate the quality of life of cancer patients after the administration of bio-bliss sryup as an add on therapyTimepoint: 4 weeks

Secondary Outcome Measures

Name	Time	Method
to evaluate changes in quality of life in cancer patient WHO and FACT G questioner changes before and after administration of interventionTimepoint: 4 weeks