Skip to content

Effectiveness of Mirror Revive Trans-Resveratrol tablets on general Health

A Consumer test to study the effects of Mirror Revive Trans-Resveratrol tablets on general health issues on Healthy Human Subjects - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/08/072576
Enrollment
100
Registered
2024-08-16
Start date
Unknown
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

None listed

Interventions

Intervention1: Trans-Resveratrol tablets: Dose: 1 pill in the morning after breakfast for 4 weeks, Route of Administration: Orally Frequency: Once a day Duration of study: 4 weeks Control Intervention

Sponsors

Miror Therapeutics Pvt Ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Voluntary man or women between 35 and 50 years. 2. Have Either of the general health issues- any digestive/cognitive/low energy levels 3. For whom the investigator considers that the compliance will be correct. 4. Cooperating, informed of the need and duration of the examinations and ready to comply with protocol procedures. 5. Having signed a Consent Form. 6.Should be able to read and write (in English, Hindi or local language). 7. Having valid proof of identity and age.

Exclusion criteria

Exclusion criteria: 1. Pregnant or nursing mothers 2.Scars, excessive terminal hair or tattoo on the studied area 3.Henna tattoo anywhere on the body (in case of studies involving hair dyes) 4.Dermatological infection or pathology on the level of studied area 5.Hypersensitivity, allergy antecedent (to any cosmetic product, raw material or hair dye) 6.Any clinically significant systemic or cutaneous disease, which may interfere with study treatment or procedures 7.Chronic illness which may influence the outcome of the study 8.Subjects on any medical treatment either systemic or topical which may interfere with the performance of the study treatment (presently or in the past 1 month) 9.Subject in an exclusion period or participating in another food, cosmetic or therapeutic trial.

Design outcomes

Primary

MeasureTime frame
Skin health Scale (0-9), Cognitive Assessment Questionnaire Score, Digestive Health Evaluation Questionnaire Score, Energy level Score(0-3)Timepoint: Day 0, Day 28

Secondary

MeasureTime frame
Not ApplicableTimepoint: Not Applicable

Countries

India

Contacts

Public ContactPuneet Mittal

CCFT Laboratories

puneetmittal@mgcts.org8937015757

Outcome results

None listed

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