Postoperative Changes in Optic Nerve Sheath Diameter in Patients

See also
Status	Clinical Trial	Phase
Completed	`NCT03041441` - Non-invasive Estimation of CSF Pressure Using MRI in Patients With Spontaneous Intracranial Hypotension	N/A
Completed	`NCT02570724` - HES Patch Versus Blood Patch	N/A
Completed	`NCT03276494` - Safety & Tolerability of Hypertonic Saline Administration Via Intraosseous Access	Phase 2

See also

Status

Clinical Trial

Phase

Completed

NCT03041441 - Non-invasive Estimation of CSF Pressure Using MRI in Patients With Spontaneous Intracranial Hypotension

N/A

Completed

NCT02570724 - HES Patch Versus Blood Patch

N/A

Completed

NCT03276494 - Safety & Tolerability of Hypertonic Saline Administration Via Intraosseous Access

Phase 2

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	NCT04301830
Study type	Observational
Source	SMG-SNU Boramae Medical Center
Contact
Status	Not yet recruiting
Phase
Start date	April 2020
Completion date	April 2022

Postoperative Changes in Optic Nerve Sheath Diameter in Patients Undergoing Spinal Anesthesia for Cesarean Delivery

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms