Interventional Study Collecting Quantitative & Qualitative Data About

Clinical Trial Description

identify wich sociocognitive factors influence the delay to go to a doctor after the emergence of first symptoms ;

Study Design

Allocation: Non-Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention

See also
Status	Clinical Trial	Phase
Recruiting	`NCT03740503` - Genomic Investigation of Unusual Responders
Not yet recruiting	`NCT06184880` - Effect of Physical Activity Program on Sedentary of Patients With Upper Aerodigestive Tract Cancer	N/A
Active, not recruiting	`NCT01505400` - Integrated Molecular Profiling in Advanced Cancers Trial

See also

Status

Clinical Trial

Phase

Recruiting

NCT03740503 - Genomic Investigation of Unusual Responders

Not yet recruiting

NCT06184880 - Effect of Physical Activity Program on Sedentary of Patients With Upper Aerodigestive Tract Cancer

N/A

Active, not recruiting

NCT01505400 - Integrated Molecular Profiling in Advanced Cancers Trial

Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.

Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.

Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

NCT number	NCT01647477
Study type	Interventional
Source	Centre Oscar Lambret
Contact
Status	Terminated
Phase	N/A
Start date	December 2012
Completion date	December 2016

Interventional Study Collecting Quantitative and Qualitative Data About Patient With Non Treated Cancer — DEREDIA

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms