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Effect of Fermented Ginseng (GINST) on Sperm Motility

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Статус
Спонзори
Jae Hoon Lee
Соработници
Ilwha Co.,Ltd.

Клучни зборови

Апстракт

This randomized, double-blind, placebo-controlled study aimed to evaluate the effect of ginseng(GINST) supplementation for 12 weeks on sperm motility.

Опис

This multicenter, randomized, double-blind, placebo-controlled clinical trial was aimed to evaluate of sperm motility improvement effect of fermented ginseng(GINST). Experimental arm and control arm were randomly assigned among the volunteers who met the inclusion criteria: men between the ages of 18 and 60 who had sperm motility of less than 32%.

To experimental arm, capsules including 160mg of fermented ginseng(GINST) ingredients will be provided for 12 weeks. To control arm, capsules of the same shape and weight as GINST capsules will be provided. These capsules are made of a cellulose component.

Primary outcome is sperm motility. Secondary outcome are , , and measured at baseline and end of the trial.

Датуми

Последен пат проверено: 05/31/2017
Прво доставено: 05/16/2017
Поднесено е проценето запишување: 06/08/2017
Прво објавено: 06/11/2017
Последното ажурирање е доставено: 06/08/2017
Последно ажурирање објавено: 06/11/2017
Крај на датумот на започнување на студијата: 01/25/2017
Проценет датум на примарно завршување: 11/30/2017
Проценет датум на завршување на студијата: 12/30/2017

Состојба или болест

Asthenozoospermia

Интервенција / третман

Dietary Supplement: GINST group

Dietary Supplement: Control group

Фаза

-

Групи за раце

РакаИнтервенција / третман
Experimental: GINST group
Experimental group was randomly assigned among the volunteers who met the inclusion criteria: men between the ages of 18 and 60 who had sperm motility of less than 32%. Fermented ginseng (GINST) was supplied.
Dietary Supplement: GINST group
Intervention group should take fermented ginseng (GINST) capsule 3 times a day, 2 capsules at one time for 12 weeks
Placebo Comparator: Control group
Control group was randomly assigned among the volunteers who met the inclusion criteria: men between the ages of 18 and 60 who had sperm motility of less than 32%. Placebo was supplied.
Dietary Supplement: Control group
Control group should take placebo capsule 3 times a day, 2 capsules at one time for 12 weeks

Критериуми за подобност

Возраст подобни за студии 18 Years До 18 Years
Полови квалификувани за студииMale
Прифаќа здрави волонтериДа
Критериуми

Inclusion Criteria:

- Male between 18 and 60 years old

- Men who have agreed to participate in this trial before the start of the study and who have written an informed consent

Exclusion Criteria:

- Those who are diagnosed and treated for hypertension (systolic blood pressure> 140mmHg and diastolic blood pressure> 90mmHg)

- Patients with a history of chemotherapy for malignant tumors

- Patients with a history of taking testosterone or antiandrogens within 1 month

- BMI> 30 or BMI <18

- Those who have the following results in the blood test: AST(aspartate aminotransferase ), ALT(Alanine transaminase) > 2 times the upper limit of reference range; Serum Creatinine> 2.0 mg / dl

- Those who ingested drugs (eg, folic acid, L-carn, HCG(human chorionic gonadotropin ), FSH(Follicle-stimulating hormone), Clomiphene, etc.) that have an effect on sperm motility within 2 weeks before the screening day.

- Persons who have received antipsychotic medication within 2 months before the screening test

- Those who have history of alcoholism or substance abuse

Исход

Мерки на примарниот исход

1. Sperm motility [Change from baseline sperm motility at 12 weeks]

Sperm motility is evaluated by Computer-Aided Semen Analysis, or CASA. Sperm motility will be expressed as '% motile' , the percent of cells that are motile. According to WHO definition, asthenozoospermia is regarded as falling below 40% motility in this study.

Секундарни мерки на исходот

1. Quality of life [Change from baseline quality of life at 12 weeks]

Quality of life was evaluated by The Short Form (36) Health Survey(SF-36 questionnaire) at baseline and 12weeks after intervention

2. Fatigue questionnaire [Change from baseline Fatigue Severity Scale at 12 weeks]

Fatigue was evaluated by Fatigue Severity Scale at baseline and 12weeks after intervention

3. Sexual function [Change from baseline Sexual Function Inventory (questionnaire) at 12 weeks]

Sexual function was evaluated by Brief Male Sexual Function Inventory (questionnaire) at baseline and 12weeks after intervention

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