Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Related Concept Videos

Nurses' Legal Responsibilities I

Nurses' Legal Responsibilities I

In healthcare, informed consent is a crucial process that involves thoroughly communicating medical treatment options to patients, including benefits, risks, potential side effects, and alternatives. This process enables patients to make well-informed decisions about their care, ensuring they understand the implications of their choices before consenting to or refusing treatment.
The legal responsibilities of a nurse regarding informed consent include the following:

Clinical Trials

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...

Clinical Trials: Overview

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...

Types of Biopharmaceutical Studies: Controlled and Non-Controlled Approaches

Types of Biopharmaceutical Studies: Controlled and Non-Controlled Approaches

Biopharmaceutical studies constitute a vital field aiming to enhance drug delivery methods and refine therapeutic approaches, drawing upon diverse interdisciplinary knowledge. In research methodologies, the choice between controlled and non-controlled studies significantly influences the study's reliability and accuracy.
Non-controlled studies, commonly employed for initial exploration, lack a control group, rendering them susceptible to biases and external influences. In contrast, controlled...

Bioavailability Study Design: Healthy Subjects Versus Patients

Bioavailability Study Design: Healthy Subjects Versus Patients

Bioavailability studies are essential for evaluating a drug's therapeutic efficacy and understanding its absorption patterns under various physiological conditions. Conducting such studies on target patient populations provides more relevant data by simulating real-world disease states. However, practical challenges often necessitate the use of young, healthy adult volunteers as study subjects.Patients may exhibit altered drug absorption patterns due to the effects of the disease itself,...

Preclinical Development: Overview

Preclinical Development: Overview

Preclinical development consists of a series of tests that ensure the safety and efficacy of a new therapeutic compound before it is tested in humans. There are four main phases to this process. First, safety pharmacology tests are conducted to ensure the drug does not produce any acutely harmful effects. These tests examine parameters such as bronchoconstriction, cardiac dysrhythmias, blood pressure changes, and ataxia. Next, preliminary toxicological testing is performed to determine the...

You might also read

Related Articles

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

Sort by

Same author

When 'winner winner chicken dinner' turned into a catastrophe: Intestinal perforation, a case of acute abdomen, a clinical case study.

Journal of minimal access surgery·2025

Same author

Compartment Syndrome Following Snake Bite.

Oman medical journal·2019

Same author

Pregnancy with sigmoid volvulus: A case report with literature review.

Turkish journal of obstetrics and gynecology·2017

Same author

A study of post-caesarean section wound infections in a regional referral hospital, oman.

Sultan Qaboos University medical journal·2014

Same author

Giant placental chorioangioma with intrauterine fetal death.

JNMA; journal of the Nepal Medical Association·2013

Same author

Idiopathic soft tissue calcification in an extremity: a case report.

Oman medical journal·2013

Search research articles

Related Experiment Video

Updated: May 20, 2026

Working with Human Tissues for Translational Cancer Research

Working with Human Tissues for Translational Cancer Research

Published on: November 26, 2015

Informed consent in clinical practice and literature overview.

Hansa Dhar¹, Dinesh Dhar

¹Department of Obstetrics and Gynaecology, Nizwa hospital, P.O. BOX 1222, 611, Nizwa, Al Dakhliya Governorate, Sultanate of Oman. hansa_dinesh2011@yahoo.com

Archives of Gynecology and Obstetrics

|July 10, 2012

Summary

Informed consent is a crucial legal and ethical requirement in healthcare. This review examines its interpretations and implications in clinical practice, considering legal and ethical factors.

More Related Videos

A Novel Method for Involving Women of Color at High Risk for Preterm Birth in Research Priority Setting

A Novel Method for Involving Women of Color at High Risk for Preterm Birth in Research Priority Setting

Published on: January 12, 2018

Using Visual and Narrative Methods to Achieve Fair Process in Clinical Care

Using Visual and Narrative Methods to Achieve Fair Process in Clinical Care

Published on: February 16, 2011

Related Experiment Videos

Last Updated: May 20, 2026

Working with Human Tissues for Translational Cancer Research

Working with Human Tissues for Translational Cancer Research

Published on: November 26, 2015

A Novel Method for Involving Women of Color at High Risk for Preterm Birth in Research Priority Setting

A Novel Method for Involving Women of Color at High Risk for Preterm Birth in Research Priority Setting

Published on: January 12, 2018

Using Visual and Narrative Methods to Achieve Fair Process in Clinical Care

Using Visual and Narrative Methods to Achieve Fair Process in Clinical Care

Published on: February 16, 2011

Area of Science:

Medical Ethics
Healthcare Law

Background:

Informed consent is a fundamental legal prerequisite for medical procedures.
Its interpretation and application vary within the current healthcare landscape.
Exceptions exist for emergency situations where consent is unobtainable.

Purpose of the Study:

To review the existing literature on informed consent.
To analyze expert inferences regarding informed consent.
To address the increasing legal and ethical considerations surrounding informed consent.

Main Methods:

Literature review of informed consent.
Analysis of expert opinions and interpretations.
Examination of legal and ethical ramifications.

Main Results:

Informed consent is a complex issue with diverse interpretations.
Legal and ethical considerations significantly influence consent practices.
Emergency exceptions are clearly defined but require careful application.

Conclusions:

A thorough understanding of informed consent is vital for healthcare professionals.
Ongoing review of legal and ethical standards is necessary.
Ensuring free and informed consent upholds patient autonomy and legal compliance.