Track this trial free. DataLookout checks ClinicalTrials.gov daily and emails you which fields changed on NCT07187427 (status, enrollment, completion dates, endpoints, sites) when this record is updated. Free accounts track up to 5 trials.

Track this trial

Incidence of Pruritus Using Intrathecal Fentanyl Versus Epidural Fentanyl to Initiate Labour Analgesia.

StatusNot Yet Recruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗

Record History

See every version on ClinicalTrials.gov ↗

  1. Eligibility criteria expanded, about 30 words
    • Secondary endpoints: details revised at 5 of 5 entries
    v2
  2. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The purpose of this study is to investigate the effect of neuraxial analgesia initiation on the incidence of pruritus in laboring women. Specifically, this study aim to compare intrathecal fentanyl with epidural fentanyl in order to determine whether the epidural route is associated with a lower occurrence and severity of pruritus. By clarifying these differences, the research seek to optimize analgesic strategies during labor while minimizing opioid-related side effects
Trial Details
NCT Number NCT07187427
Lead Sponsor St. Justine's Hospital
Conditions
(from sponsor)		 Pruritis, Hypotension Drug-Induced, Urinary Retention, Fetal Bradycardia During Labor, Nausea and Vomitting, Satisfaction, Patient, Labor Analgesia, Neuraxial Opioid +4 more
Related terms Hypotension, Nausea, Patient Satisfaction, Pruritus, Urinary Retention
Enrollment 80 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov