Sleep in Hospitalized Children at MSKCC

See also
Status	Clinical Trial	Phase
Recruiting	`NCT02644993` - Registry for Analysis of Quality of Life, Normal Organ Toxicity and Survival of Pediatric Patients Treated With Proton Therapy	N/A
Not yet recruiting	`NCT04873284` - Comparative Study of Fosaprepitant and Aprepitant for the Prevention of Chemotherapy-induced Nausea and Vomiting in Pediatric Caner Patients	N/A
Recruiting	`NCT04831359` - Tissue Doppler Assessment of Right Ventricle Function in Pediatrics Underwent Chemotherapy

See also

Status

Clinical Trial

Phase

Recruiting

NCT02644993 - Registry for Analysis of Quality of Life, Normal Organ Toxicity and Survival of Pediatric Patients Treated With Proton Therapy

N/A

Not yet recruiting

NCT04873284 - Comparative Study of Fosaprepitant and Aprepitant for the Prevention of Chemotherapy-induced Nausea and Vomiting in Pediatric Caner Patients

N/A

Recruiting

NCT04831359 - Tissue Doppler Assessment of Right Ventricle Function in Pediatrics Underwent Chemotherapy

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	NCT02836041
Study type	Observational
Source	Memorial Sloan Kettering Cancer Center
Contact
Status	Completed
Phase
Start date	July 7, 2016
Completion date	May 26, 2021

Sleep in Hospitalized Children at MSKCC

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms