Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Legal Guidelines for Documentation01:06

Legal Guidelines for Documentation

The legal guidelines for nursing documentation are essential for ensuring accurate, professional, and ethical recording of patient care. The guidelines are discussed here:
Clinical Trials: Overview01:11

Clinical Trials: Overview

Clinical development focuses on how the drug will interact with the human body and encompasses four key phases of clinical trials, each serving a specific purpose in assessing the safety and effectiveness of new drugs. These phases overlap and build upon one another. Phase I involves a small group of healthy volunteers (typically 20-80 individuals) or, in cases where significant toxicity is expected, patients with the targeted disease, such as cancer or AIDS. The volunteers are tested for...
Clinical Trials01:16

Clinical Trials

Clinical trials are prospective experimental studies conducted on humans to determine the safety and efficacy of treatments, drugs, diet methods, and medical devices. Using statistics in clinical trials enables researchers to derive reasonable and accurate conclusions from the collected data, allowing them to make wise decisions in uncertain situations. In medical research, statistical methods are crucial for preventing errors and bias.
There are four phases in a clinical trial. A phase one...
Introduction to Documentation and Reporting01:20

Introduction to Documentation and Reporting

Documentation is the systematic process of formally recording, maintaining, and communicating information.
Nursing documentation records essential information and details regarding a patient's care and treatment in written or electronic form. It is a critical aspect of nursing practice that involves documenting assessments, interventions, outcomes, and other relevant details about a patient's health status.
Documentation maps the patient's health journey by creating a comprehensive and precise...
Standards of Care II01:19

Standards of Care II

Nurses bear specific legal responsibilities under several federal statutes, including:
Purpose of Health Records II01:19

Purpose of Health Records II

Health records serve various essential purposes in the healthcare system. Here are some key purposes:

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Recommendations for the DesIgn of sham acupuncture in RandomizEd Controlled Trials (the DIRECT guidelines).

Journal of integrative medicine·2026
Same author

SARS-CoV-2 Spike Protein as a Target of the COVID-19 Vaccine Disrupts Insulin Signaling in Type 2 Diabetes.

MedComm·2025
Same author

Regulatory frameworks and evidence requirements for traditional, complementary and integrative medicines.

Bulletin of the World Health Organization·2025
Same author

MT1-MMP inhibition rejuvenates ageing brain and rescues cognitive deficits in obesity.

Cell discovery·2025
Same author

International clinical practice guideline on the use of traditional Chinese medicine for functional dyspepsia (2025).

Journal of integrative medicine·2025
Same author

Bridging the Gap: A Comprehensive Study on Traditional Chinese Medicine Strategies for Managing Adult Irritable Bowel Syndrome.

The American journal of Chinese medicine·2024
Same journal

Compression therapies for the treatment of venous leg ulcers: a mixed method process evaluation in a randomised controlled trial, VenUS6.

Trials·2026
Same journal

Cheek acupuncture for enhancing postoperative recovery after endoscopic sinus surgery: study protocol for a pilot randomized controlled trial.

Trials·2026
Same journal

Methodological guidance for incorporating lived experience in the early stages of core outcome set development: a scoping review.

Trials·2026
Same journal

IMPACT-Introduction of Mycotic Prophylaxis At Cystectomy Trial: perioperative mycotic prophylaxis with fluconazole to reduce postoperative complications following cystectomy-study protocol for a national multi-center, double-blinded, placebo-controlled, randomized clinical trial.

Trials·2026
Same journal

A cluster randomized trial to evaluate the effects of a quality cluster-based intervention on the use of prostate-specific antigen test in general practice-a study protocol.

Trials·2026
Same journal

Adjunctive optical and magnetic stimulation for venous and mixed etiology leg ulcers: protocol for the NAZARÉ multicenter randomized controlled trial.

Trials·2026
See all related articles

Related Experiment Video

Updated: Jun 12, 2026

Establishment of a Clinic-based Biorepository
07:50

Establishment of a Clinic-based Biorepository

Published on: May 29, 2017

Legislation for trial registration and data transparency.

Zhao-Xiang Bian1, Tai-Xiang Wu

  • 1School of Chinese Medicine, Hong Kong Baptist University, Hong Kong, China. bzxiang@hkbu.edu.hk

Trials
|May 28, 2010
PubMed
Summary
This summary is machine-generated.

Ensuring clinical trial transparency requires robust enforcement. Legislation and a global network are proposed to mandate trial registration and accurate data dissemination, rebuilding public trust.

More Related Videos

Biobank for Translational Medicine: Standard Operating Procedures for Optimal Sample Management
08:01

Biobank for Translational Medicine: Standard Operating Procedures for Optimal Sample Management

Published on: November 30, 2022

Related Experiment Videos

Last Updated: Jun 12, 2026

Establishment of a Clinic-based Biorepository
07:50

Establishment of a Clinic-based Biorepository

Published on: May 29, 2017

Biobank for Translational Medicine: Standard Operating Procedures for Optimal Sample Management
08:01

Biobank for Translational Medicine: Standard Operating Procedures for Optimal Sample Management

Published on: November 30, 2022

Area of Science:

  • Biomedical Research Ethics
  • Clinical Trial Management
  • Data Transparency

Background:

  • Erosion of public confidence in clinical trials due to data suppression and manipulation.
  • Previous attempts at universal trial registration (e.g., Declaration of Helsinki, WHO ICTRP) lacked enforcement power.
  • Need for effective mechanisms to ensure accurate and timely dissemination of clinical trial data.

Discussion:

  • Legislation is the most effective means to enforce trial registration and data transparency.
  • Proposing a two-step approach for global implementation.
  • Highlighting the USA's FDAAA Act 2007 as a legislative precedent.

Key Insights:

  • Universal trial registration and data transparency are crucial for public trust.
  • Enforcement is key to the success of registration initiatives.
  • A legislative framework combined with a global network can ensure compliance.

Outlook:

  • Establishment of a global network for consistent policy and enforcement.
  • Future efforts should focus on international collaboration for trial data integrity.
  • Strengthening regulatory frameworks to promote ethical research practices.