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A clinical study to evaluate the effect of BCO-5 on safety ,sleep, stress and immunity in Healthy Subjects with Sleep Deprivation

A Randomized, Multi Center, Double Blinded, Placebo-Controlled, Parallel-Group, Comparative Clinical Study to Evaluate the Safety and Efficacy of BCO-5 on Sleep Quality and Immunomodulatory Support in Healthy Subjects with Sleep Deprivation.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/05/033780
Enrollment
70
Registered
2021-05-25
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: BCO-5: Oral administration of single BCO-5 capsule for 90 days Control Intervention1: Placebo: Oral administration of single Placebo capsule for 90 days

Sponsors

Akay Natural Ingredients Pvt Ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.PSQI score greater than 5 2. Perceived Stress Scale greater than 14 3. Generally healthy subjects with body weight greater than 50kg. 4. Women of child bearing potential practicing an acceptable method of birth control as judged by the investigator(s) [such as condoms, foams, jellies, diaphragm, intrauterine device, oral or long acting injected contraceptives]. 5. Should be ready to abstain from alcohol consumption, smoking and consumption of caffeinated beverages. 6. Must be willing and able to give informed consent and comply with the study procedures

Exclusion criteria

Exclusion criteria: 1. Subjects suffering from any chronic health conditions (e.g. diabetes, hypertension, chronic renal failure, heart, thyroid and liver disease) requiring medical treatment 2. Hepatic impairment (Alanine transaminase/Aspartate transaminase levels less than 3 upper limit of normal) or renal impairment (serum creatinine less than 2.0 mg/dl) 3.History of Chronic metabolic disease, Psychiatric illness, Drug abuse, smoking, abuse/addiction to alcohol, Endocrine abnormalities including stable thyroid disease Cardiovascular surgery / History of any major surgery 4. Subjects having symptoms of viral infection, including COVID-19 infection 5. Known HIV or Hepatitis B positive or any other immuno-compromised state 6. Pregnant and lactating women 7. Subjects allergic to Herbal Nutra or Pharmaceutical products 8. Currently participating or having participated in another clinical trial during the last 1 month prior to the beginning of this study 9. Any additional condition(s) that in the Investigators opinion would warrant exclusion from the study or prevent the subject from completing the study.

Design outcomes

Primary

MeasureTime frame
The Safety of BCO-5Timepoint: Day 0, Day 45, Day 90

Secondary

MeasureTime frame
Changes in Bio MarkersTimepoint: Day 45, Day 90;Changes In Questionnaire based assessmentsTimepoint: Day 0, Day 45, Day 90;Changes in Stress levelTimepoint: Day 0, Day 45, Day 90

Countries

India

Contacts

Public ContactJestin V Thomas

Leads Clinical Research and Bio Services Pvt. Ltd

jestin.leadsclinbio@gmail.com9845125293

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026