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Effect of Fermented Prunus Mume Vinegar on Improvement of Fatigue

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StaatusVärbamine
Sponsorid
Pusan National University Yangsan Hospital

Märksõnad

Abstraktne

The investigators conduct a randomized, double-blind, placebo-controlled study to investigate the effects of Fermented Prunus Mume Vinega on Improvement of Fatigue in adults for 8 weeks.

Kirjeldus

Previous studies have indicated that Fermented Prunus Mume Vinega may have the ability to improve fatigue. Therefore, the investigators conduct a randomized, double-blind, placebo-controlled study to investigate the effects of tFermented Prunus Mume Vinega on Improvement of Fatigue in adults; the safety of the compound are also evaluate. The Investigators examine fatigue severity scale, lactate, creatinine kinase, urinary malondialdehyde at baseline, as well as after 4 and 8 weeks of intervention. Sixty adults were administered either 600 mg of Fermented Prunus Mume Vinega or a placebo each day for 8 weeks;

Kuupäevad

Viimati kinnitatud: 02/29/2020
Esmalt esitatud: 03/20/2020
Hinnanguline registreerumine on esitatud: 03/22/2020
Esmalt postitatud: 03/23/2020
Viimane värskendus on esitatud: 03/22/2020
Viimati värskendus postitatud: 03/24/2020
Õppe tegelik alguskuupäev: 03/18/2020
Eeldatav esmane lõpetamise kuupäev: 12/29/2020
Eeldatav uuringu lõpetamise kuupäev: 12/30/2020

Seisund või haigus

Fatigue

Sekkumine / ravi

Dietary Supplement: Fermented Prunus Mume Vinegar group

Dietary Supplement: Placebo group

Faas

-

Käerühmad

ArmSekkumine / ravi
Experimental: Fermented Prunus Mume Vinegar group
This group takes Fermented Prunus Mume Vinegar for 8 weeks.
Dietary Supplement: Fermented Prunus Mume Vinegar group
This group takes Fermented Prunus Mume Vinegar for 8 weeks
Placebo Comparator: Placebo group
This group takes placebo for 8 weeks.
Dietary Supplement: Placebo group
This group takes placebo for 8 weeks.

Abikõlblikkuse kriteeriumid

Õppimiseks sobivad vanused 19 Years To 19 Years
Uuringuks kõlblikud soodAll
Võtab vastu tervislikke vabatahtlikkeJah
Kriteeriumid

Inclusion Criteria:

- Those who complain of fatigue for more than 1 month

- Fatigue Severity Scale 3 points or more

Exclusion Criteria:

- chronic hepatitis B or C infection

- being treated for hypothyroidism or hyperthyroidism

- more than twice the normal upper limit of Creatinine

- Liver enzyme value is more than twice the normal upper limit

- Uncontrolled diabetes (over 160 mg / dl of fasting blood sugar)

- Uncontrolled hypertension (more than 160/100 mmHg, measured after 10 minutes of stability in subjects) or those with heart disease, such as angina or myocardial infarction

- taking medications that affect fatigue within the past 1 month (psychiatric drugs such as Chinese medicine, soy drugs, depression, beta-blockers, steroids, hormones, etc.). However, intermittent medication due to sleep disorders is excluded.

- a history of gastrointestinal resection or complain of severe gastrointestinal symptoms such as heartburn and indigestion

- already have participated in or plan to participate in another drug clinical trial

- Alcohol abusers

- pregnant, lactating or have a pregnancy plan during the clinical trial period

- allergic reactions to Fermented Prunus Mume Vinegar

- A person deemed inappropriate by the researcher for other reasons

Tulemus

Esmased tulemusnäitajad

1. Fatigue severity scale [8 weeks]

Fatigue severity scale, minimum~maximum values (1~7), higher scores mean a worse outcome.

Sekundaarsed tulemusmõõdud

1. Lactate level [8 weeks]

Lactate level (mg/dL)

2. Creatinine kinase level [8 weeks]

Creatinine kinase level (IU/L)

3. Urinary malondialdehyde level [8 weeks]

Urinary malondialdehyde level (mmol/mg Cr)

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