UnknownPhase 1

Herb Drug Interaction of Traditional Chinese Herb and Commonly Used Drugs

Taiwan50 participantsStarted 2008-12

Plain-language summary

The purpose of this study was to investigate a possible response to nalbuphine (Nubian) and morphine with traditional Chinese herbs in healthy volunteers.

Who can participate

Age range

20 Years – 40 Years

Sex

FEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Normal healthy adult subjects between 20-40 years of age * Body weight within 80-120% of ideal body weight * Acceptable medical history, physical examination and clinical laboratory determinations Exclusion Criteria: * Recent history of drug or alcohol addiction or abuse * Donating greater than 150 ml of blood within two months prior to Period I * Taking any prescription medication or any nonprescription medication within 14 days prior to Period I doing * Receiving any investigational drug within 30 days prior to Period I dosing * Taking any drug known to induce or inhibit hepatic drug metabolism within 30 days prior to the beginning of the study * Any clinically significant diseases * History of allergic response to nalbuphine or related drugs and traditional Chinese herbs

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

The pharmacokinetic parameters

Timeframe: 24 hours

Trial details

NCT IDNCT00923000

SponsorTri-Service General Hospital (TSGH)

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2009-12

Contact for this trial

Yu-Rong Li

886-2-87923311 crccrc@ndmctsgh.edu.tw

View on ClinicalTrials.gov More Healthy trials