Pilot studies and feasibility trials form a critical component of the clinical research process by enabling investigators to assess the practicality of study protocols on a smaller scale prior to ...
Stability studies measure how medical devices respond to environmental stresses such as temperature, humidity, light, and ...
Protocols.io is an online platform designed for researchers to share their lab protocols and methodology as step-by-step instructions. Here, we share some of their latest protocols for preparing ...
Background Complex breast surgery, including immediate breast reconstruction and oncoplastic procedures, is increasingly performed to optimise oncologic and aesthetic outcomes. Postoperative wound ...
A protocol deviation or violation is any departure from the study procedures or treatment plans as specified in the IRB-approved protocol. Protocol deviations occur when an investigator does not ...
Follow the step-by-step instructions below to successfully maintain and close a protocol with the IRB. Instructions below include information about continuing reviews, amendments, event reporting (new ...
The purpose of this guidance is to explain the roles and responsibilities of both undergraduate and graduate students when submitting protocols to be reviewed by the Institutional Review Board (IRB).
Ethics and Clinical Research: Improving Transparency and Informed Consent in Phase I Oncology Trials
Radiotherapy or Surgery of the Axilla After a Positive Sentinel Node in Breast Cancer: 10-Year Results of the Randomized Controlled EORTC 10981-22023 AMAROS Trial Informed consent is a basic ethical ...
In a recent study published in Nature Medicine, researchers created the REP-EQUITY toolbox for capturing an equitable and representative sample for health research studies. Research participants are ...
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