Lime Powder Regimen in Healthy Volunteers

NCT ID: NCT01273025

Last Updated: 2011-01-10

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE1
• Total Enrollment: 15 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2010-12-31
• Study Completion Date: 2011-03-31

Brief Summary

The study aims to investigate the pharmacokinetic parameters and its antioxidative effects in Thai healthy men.

Conditions

Kidney Stone; Oxidative Stress

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: BASIC_SCIENCE
• Blinding Strategy: NONE

Interventions

Lime powder regime

1 sachet of lime powder regimen with 200 ml of water

Intervention Type: DIETARY_SUPPLEMENT

Eligibility Criteria

Inclusion Criteria

• Thai healthy male or female aged 18-45 years old
• BMI 18-25 kg/m2
• Normal medical history, physical examination and vital signs
• Normal screening laboratories
• no history of drug allergies
• Willingness to take part in the study and provide informed consent

Exclusion Criteria

• History of GI, liver, kidney, allergic disease or any other disease that may interfere with the bioavailability of lime powder regimen
• History of alcohol or drug abuse
• Heavy smoking
• Receive any medication within 14 days prior to the study day

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 45 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Chulalongkorn University

OTHER

Sponsor Role: lead

Responsible Party

Chulalongkorn University

Principal Investigators

Poonsin Poungpairoj, BSc

Role: PRINCIPAL_INVESTIGATOR

Chulalongkorn University

Locations

Chula clinical research center

Bangkok, , Thailand

Countries

Thailand

Other Identifiers

PPK-10-003

Identifier Type: -

Identifier Source: org_study_id