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Effects of Oral Ingestion of Drinking Water Using a Tumbler That Emits Far Infrared Rays on Metabolic Profile

Effects of Oral Ingestion of Drinking Water Using a Tumbler That Emits Far Infrared Rays at Room Temperature on Metabolic Profile in Adults: a RCT

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03920436
Enrollment
30
Registered
2019-04-18
Start date
2019-02-01
Completion date
2019-07-31
Last updated
2019-09-11

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

Conditions

Metabolic Problems

Brief summary

The investigators conduct a randomized, double-blind, placebo-controlled study to investigate the effects of oral ingestion of drinking water using a tumbler that emits far infrared rays at room temperature on metabolic profile in adults for 8 weeks.

Detailed description

The investigators conduct a randomized, double-blind, placebo-controlled study to investigate the effects of oral ingestion of drinking water using a tumbler that emits far infrared rays at room temperature on metabolic profile in adults for 8 weeks; the safety of the compound are also evaluate. The Investigators examine lipid profile, glucose, liver and renal function at baseline, as well as after 4, 8 weeks of intervention. Thirty adults were administered either 1.8 L of drinking water using a tumbler that emits far infrared rays at room temperature or drinking water using a sham-tumbler each day for 12 weeks.

Interventions

DIETARY_SUPPLEMENTinfrared water group

This group takes 1,8 L of drinking water using a tumbler that emits far infrared rays at room temperature.

DIETARY_SUPPLEMENTsham group

This group takes 1,8 L of drinking water using a tumbler at room temperature.

Sponsors

Pusan National University Yangsan Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
19 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* 19 years and older

Exclusion criteria

* aspartate aminotransferase (AST) or alanine aminotransferase (ALT) more than twice the highest reference value * serum creatinine ≥ 1.5 mg/dL) * uncontrolled diabetes mellitus (a fasting glucose of \>160 mg/dL) * uncontrolled hypertension (BP \> 160/100 mmHg) * severe gastrointestinal symptoms * alcohol abuser * pregnant or lactating women * allergic to the ingredient involved * cardiocebrovascular diseases or any cancer during the six months prior to study * smoker

Design outcomes

Primary

MeasureTime frameDescription
Low density lipoprotein cholesterol (LDL-C)Change from baseline level of LDL-C at 8 weeksChange of LDL-C during 8 weeks

Secondary

MeasureTime frameDescription
alanine transaminase (ALT)Change from baseline level of ALT at 8 weeksChange of ALT during 8 weeks
homeostasis model assessment of insulin resistance (HOMA-IR)Change from baseline level of HOMA-IR at 8 weeksChange of HOMA-IR during 8 weeks
free fatty acidChange from baseline level at 8 weeksChange of free fatty acid during 8 weeks
aspartate transaminase (AST)Change from baseline level of AST at 8 weeksChange of AST during 8 weeks
creatinineChange from baseline level of creatinine at 8 weeksChange of creatinine during 8 weeks
body weightChange from baseline level at 8 weeksChange of body weight during 8 weeks

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026