Viewing Study NCT01126294


Ignite Creation Date: 2025-12-25 @ 2:00 AM
Ignite Modification Date: 2025-12-26 @ 12:24 AM
Study NCT ID: NCT01126294
Status: UNKNOWN
Last Update Posted: 2010-05-19
First Post: 2010-05-17
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Perioperative Melatonin in Lumbar Laminectomy
Sponsor: University Health Network, Toronto
Organization:

Study Overview

Official Title: Perioperative Analgesic and Anxiolytic Effect of Melatonin in Patients Undergoing Lumbar Laminectomy
Status: UNKNOWN
Status Verified Date: 2010-04
Last Known Status: RECRUITING
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Patients undergoing lumbar laminectomy surgery will receive either 5 or 10 mg melatonin or placebo once the evening before surgery and again 90 minutes before surgery. Pain and anxiety will be assessed over the 24 hour period following surgery.
Detailed Description: None

Study Oversight

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