Viewing Study NCT01342835


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Study NCT ID: NCT01342835
Status: UNKNOWN
Last Update Posted: 2011-04-27
First Post: 2011-04-20
Is NOT Gene Therapy: False
Has Adverse Events: False

Brief Title: Postoperative Analgesia in Children After Propofol Anesthesia
Sponsor: University Clinical Centre of Kosova
Organization:

Study Overview

Official Title: Postoperative Analgesia in Children After Propofol Anesthesia
Status: UNKNOWN
Status Verified Date: 2010-09
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: propan
Brief Summary: The investigators hypothesize that patients anesthetized with sevoflurane have more pain, postoperatively, than those anesthetized with propofol.
Detailed Description: In a randomize, prospective, double-blind study, the subjects are 100 premedicated children, aged 3 to 6 years, who undergo one type of surgical procedure, hernia repair surgery. Anesthesia is maintains with propofol anesthesia (group P, n=50) or with sevoflurane anesthesia (group S, n=50). and fentanyl administered during surgery. Faces Pain Scale (FPS) is use to assess pain severity.

Study Oversight

Has Oversight DMC: True
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?:

Secondary ID Infos

Secondary ID Type Domain Link View
RAA12 REGISTRY RAA12 View