Evaluation of Antral Ultrasonography for Full Stomach Diagnosis Before

Clinical Trial Description

n/a

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic

See also
Status	Clinical Trial	Phase
Not yet recruiting	`NCT06320574` - Nurses' Competence in Gastric Ultrasound
Recruiting	`NCT05763745` - Bedside Ultrasonic Assessment for Gastric Content in Patients With Upper GI Bleeding Undergoing Endoscopy: a Pilot Study	N/A
Recruiting	`NCT05728242` - Point-of-care Gastric Ultrasound for Fracture Surgery

See also

Status

Clinical Trial

Phase

Not yet recruiting

NCT06320574 - Nurses' Competence in Gastric Ultrasound

Recruiting

NCT05763745 - Bedside Ultrasonic Assessment for Gastric Content in Patients With Upper GI Bleeding Undergoing Endoscopy: a Pilot Study

N/A

Recruiting

NCT05728242 - Point-of-care Gastric Ultrasound for Fracture Surgery

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	NCT02936882
Study type	Interventional
Source	Hôpital Necker-Enfants Malades
Contact
Status	Recruiting
Phase	N/A
Start date	March 2016

Evaluation of Antral Ultrasonography for Full Stomach Diagnosis Before Pediatric Surgical Emergencies

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms