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a clinical trial to study the efficacy of Chlorophytum borivilianum on physical performance in response to exercise (physical stress) in healthy adults

â??A prospective, randomized, placebo controlled, double blind comparative, pilot study to evaluate the efficacy of Chlorophytum borivilianum on physical performance in response to exercise (physical stress) in healthy adultsâ??

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/08/009586
Enrollment
60
Registered
2017-08-31
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: Chlorophytum borivilianum: Cap.Chlorophytum borivilianum ,500mg,TDS,2 months Control Intervention1: Maize starch: Cap.Maize starch,500mg,TDS,2 months

Sponsors

Dr Raaakhi Tripathi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Volunteers with normal health status which will be assessed by below-mentioned investigations: A) Clinical history and examination B) Hematological: Hb, CBC & ESR C) Biochemical: LFT, RFT 2. Volunteers ready to refrain from unaccustomed strenuous physical activity at least 1 week before starting the study & throughout the study duration & those who do not drink & smoke( atleast for past 6 months) 3. Volunteers with no h/o any lower limb OR upper limb injury within past six months. 4. Volunteers who were ready to abide by trial procedures and to give a written informed consent

Exclusion criteria

Exclusion criteria: 1. Volunteers with H/o of allergy or intolerance to herbal drugs 2. Volunteers with H/o intake of traditional systems of medicine including drugs with rasayana properties 3. Pregnant and lactating woman 4. Volunteers taking anabolic steroids, protein supplements or other nutritional supplements and use of any recreational drug or a history of drug addiction 5. Volunteers suffering from any cardiovascular, musculoskeletal, hepatobiliary, genitourinary, neurological or any psychiatric condition and on any chronic medication 6. Volunteers with H/o of any illness which might confound the results of the study or poses an additional risk to the participant 7. Volunteers who have recently joined gymnasium in past one month and /or were doing active resistance exercises

Design outcomes

Primary

MeasureTime frame
exercise protocol will be followed on cycle ergometer ,variables will be measured after 6 minute exercise test on cycle ergometer. i.Total distance travelled ii.Maximum speed iii.Average speed Timepoint: it will be recorded on 1st visit(day 0),2nd visit (day 30) ,third visit(day 60)

Secondary

MeasureTime frame
Following tests will be done to measure the secondary outcomes 1)6 minute walk test i.Distance travelled in 6 minutes ii.HR(at the end of test) iii.BP(at the end of test) 2)Fixed workload exercise on cycle ergometer i.SBP ii.DBP iii.HRavg (these readings will be taken at the end of 4, 5 &6 minutes and average of these readings will be taken) 3)Hand grip strength by Jammers hand held dynamometer Average of 3 readings.Timepoint: it will be recorded on 1st visit(day 0),2nd visit (day 30) ,third visit(day 60)

Countries

India

Contacts

Public ContactDr Pradnya Dethe

Seth G.S.Medical College,KEM Hospital

drpradnya.04@gmail.com9969848473

Outcome results

None listed

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