Viewing Study NCT04645823


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Ignite Modification Date: 2025-12-18 @ 8:16 AM
Study NCT ID: NCT04645823
Status: None
Last Update Posted: 2024-04-24 00:00:00
First Post: 2020-11-22 00:00:00
Is Possible Gene Therapy: False
Has Adverse Events: False

Brief Title: Spinal Fentanyl or Epidural Analgesia in the Early First Phase of Induced Labor
Sponsor: None
Organization:

Study Overview

Official Title: Spinal Fentanyl or Epidural Analgesia in the Early First Phase of Induced Labor
Status: None
Status Verified Date: 2024-04
Last Known Status: None
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: A total of 60 parturients undergoing induction of labour will be consented to participate in the study where they will be randomized to receive either spinal fentanyl (20 µg) or epidural analgesia (fentanyl 100µg and lidocaine 80 mg).

They will be monitored for the development of analgesia for a duration of 30 minutes.
Detailed Description: None

Study Oversight

Has Oversight DMC: None
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?: