Biotin Sample Collection Study

Swiss Precision Diagnostics (SPD)

Status: Completed

Conditions: Healthy Volunteers; Biotin Excretion

Treatments: Dietary Supplement: Biotin

Study type: Interventional

Funder types: Industry

Identifiers

NCT03746821

PROTOCOL-1001

Details and patient eligibility

About

This protocol has been designed for a collection of urine samples from volunteers who will be given high dose biotin supplements over a period of 5 days, in order to provide a research sample bank to examine for biotin excretion rates

Full description

This is a sample collection study from a minimum of 10 volunteers who will be required to take a Biotin supplement daily for a period of 5 days.

Each volunteer will be asked to read the volunteer information sheet and if they wish to participate in the study, the study admission form will be completed and the volunteer will be asked to sign a consent form.

After informed consent each volunteer will be assigned a unique volunteer number for the duration of the trial to provide anonymity. The volunteer will be provided with a daily diary, urine collection material and a full set of volunteer instructions.

The daily diary will collect the following information;

• Date
• Whether or not supplement was taken and time taken
• sample collection times during the day

Volunteers will be requested to:

Day 1: Collect a urine sample from every void during the day. Days 2-6: Take biotin supplements with their evening meal and collect a urine sample from every void during the day Day 7: Collect a urine sample from every void during the day

All samples will be stored in the SPD Bio-bank until required for analysis.

Enrollment: 12 patients

Sex: Female

Ages: 18 to 45 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Willing to take biotin supplements and collect urine samples
• Has regular menstrual periods
• SPD employee or partner of SPD employee

Exclusion criteria

• Taking any other supplements or medication (other than contraceptive pill)
• Taken Antibiotics in the last 4 weeks
• Diagnosed with metabolic disorder, kidney or liver disease
• Known Pregnancy or seeking to conceive
• Breast feeding
• Undergoing medical investigation for hormone imbalance
• Condition that contra-indicates pregnancy
• Condition that contra-indicates use of biotin supplements

Trial design

Primary purpose: Basic Science

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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12 participants in 1 patient group

Biotin

Other group

Description:

Volunteers to take biotin suppliment

Treatment:

Dietary Supplement: Biotin