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CODEPAD (Collaborative Outcomes of DEpression and Pain Associated With Delivery)

Study acronym: CODEPAD
StatusActive, Not Recruiting
PhasePhase 2/3
Started
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Record History

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  1. Study completion pushed from Dec 31, 2026 to Dec 31, 2027v15
  2. Study completion date: Dec 31, 2025 to Dec 31, 2026v14
  3. Study completion date: Dec 31, 2024 to Dec 31, 2025
    • Publications: 6 to 7
    v13
  4. Study completion date: Dec 31, 2023 to Dec 31, 2024v12
  5. Study completion date: Dec 31, 2022 to Dec 31, 2023v11
Show 9 earlier versionsHide 9 earlier versions
  1. Secondary endpoints: 10 to 11v10
  2. Primary endpoints: 1 to 2v9 Show 6 more changesShow less
    • Trial status: Recruiting to Active, Not Recruiting
    • Enrollment target: estimated 1326 to confirmed 881
    • Primary completion date changed from estimate of Aug 31, 2021 to Jul 19, 2021
    • Secondary endpoints: 8 to 10
    • Study description expanded, about 26 words
    • Site details revised
  3. Secondary endpoints: 7 to 8v8
  4. Primary completion date: May 31, 2021 to Aug 31, 2021
    • Study completion date: Dec 31, 2021 to Dec 31, 2022
    v7
  5. Primary completion date: Jan 16, 2020 to May 31, 2021
    • Study completion date: Mar 16, 2020 to Dec 31, 2021
    v6
  6. 2 versions Re-verified since Aug 22, 2018, no change to tracked fieldsv4-v5
  7. Trial status: Not Yet Recruiting to Recruiting
    • Start date changed from estimate of Jun 5, 2017 to Jun 15, 2017
    • Site details revised
    v3
  8. Start date: May 24, 2017 to Jun 5, 2017v2
  1. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
Postnatal depression affects about 10-15% of women after childbirth. Approximately 3-5% of women experience a moderate-to-severe depression that requires medical attention. This study aims to investigate the implication of pain relief choice in reducing the postnatal depression of women who deliver their babies.
Trial Details
NCT Number NCT03167905
Lead Sponsor KK Women's and Children's Hospital
Conditions
(from sponsor)		 Depression, Postpartum, Analgesia, Obstetrical, Anesthesia, Obstetrical
Related terms Agnosia, Depression, Postpartum
Enrollment 881 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov