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QIPB in Inguinal Hernia

StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Record status
This record was last updated March 11, 2026 (before its estimated June 1, 2026 completion). Its status may not reflect the trial's current state.

Record History

  1. Minor Re-verified, no change to tracked fieldsv6
  2. Notable Primary and study completion dates: Nov 30, 2025 to Jun 1, 2026v5
  3. Minor Primary and study completion dates: Aug 30, 2025 to Nov 30, 2025v4
  4. Minor Primary and study completion dates: Jun 23, 2025 to Aug 30, 2025v3
  5. Notable Trial status: Not Yet Recruiting to Recruiting
    • Primary and study completion dates: Apr 10, 2025 to Jun 23, 2025
    • Start date changed from estimate of Mar 10, 2025 to Mar 23, 2025
    v2
  6. Minor 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
Inguinal hernia repair is one of the most commonly performed surgical procedures. It is generally performed under regional anesthesia techniques, such as local anesthesia, peripheral nerve blocks, or neuraxial anesthesia (spinal or epidural anesthesia), or under general anesthesia. Despite various available analgesic regimens, numerous studies have demonstrated that postoperative pain control remains inadequate. Opioids, nonsteroidal anti-inflammatory drugs, and analgesics are frequently used for postoperative pain management. However, these medications are associated with uncertain efficacy and undesirable side effects. Pain is a critical factor in the postoperative period, contributing to delayed ambulation and paralytic ileus, ultimately hindering early discharge.
Trial Details
NCT Number NCT06862609
Lead Sponsor Konya City Hospital
Conditions
(from sponsor)
Postoperative Pain
Related terms Postoperative Pain
Enrollment 70 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov