Viewing Study NCT01062893


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Study NCT ID: NCT01062893
Status: TERMINATED
Last Update Posted: 2018-10-16
First Post: 2010-02-01
Is Gene Therapy: True
Has Adverse Events: True

Brief Title: Combined Spinal/Epidural (CSE) Saline Duration/Spread
Sponsor: Wake Forest University Health Sciences
Organization:

Study Overview

Official Title: Effect of Epidural Saline on Duration and Spread of Subsequent Spinal Analgesia/Anesthesia Using a CSE Technique
Status: TERMINATED
Status Verified Date: 2018-10
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: lack of subjects and manpower issues
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: An attempt is being made to see if by injecting a set volume of sterile saline into the epidural space during the treatment of labor pain with a combined spinal/epidural (CSE) increases the amount of pain relief obtained and makes the labor analgesia lasts longer. Subjects are in the study from the time their CSE is placed until they request additional pain medication from the spinal dose of numbing medicine wearing off.
Detailed Description: None

Study Oversight

Has Oversight DMC: True
Is a FDA Regulated Drug?: True
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: