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Quality of Postoperative Analgesia and Functional Recovery After Elective Cesarean Delivery

Study acronym: MoFe
StatusRecruiting
PhaseNot applicable
Started
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Record History

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  1. Primary completion date: Aug 31, 2025 to Dec 31, 2027
    • Study completion date: Sep 1, 2025 to Dec 31, 2027
    v4
  2. Trial status: Not Yet Recruiting to Recruiting
    • Study sites: 0 to 1
    • Start date changed from estimate of Apr 1, 2024 to Jun 12, 2024
    v3
  3. Secondary endpoints revised (7)v2
  4. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
Based on randomization, patients will receive a mixture for spinal anesthesia and will be followed in the following hours for the various outcomes and for functional recovery
Trial Details
NCT Number NCT06355271
Lead Sponsor Ente Ospedaliero Cantonale, Bellinzona
Conditions
(from sponsor)		 Obstetric Pain
Related terms Labor Pain
Enrollment 63 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov