drugset / Trial / NCT03244540

Regional Analgesia After Cesarean Section

NCT03244540 ↗

Phase 4 Completed 105 enrolled Medical University of Lublin
RandomizedParallel-groupTriple-blindTreatment

Summary

All patients will be anaesthetized with spinal technique. Each patient will be treated with intravenous morphine - patient controlled analgesia (PCA). 2 of 3 groups of patients will receive ultrasound-guided transversus abdominis plane or quadratus lumborum block to treat postoperative pain. Postoperative pain will measured with visual-analogue scale (VAS). Total morphine consumption and time to the first demand will be noted. 1, 2, 6 months after surgery each patient will be called to assess neuropathic pain with Neuropathic Pain Symptom Inventory (NPSI).

Timeline

Start
2017-09-04
Primary completion
2018-10-29
Completion
2019-08-30

Outcome

Met primary endpoint

paper At rest, the pain intensity was significantly higher in the CON group than in the QLB and TAPB groups at hours two and eight. PMID 33800559 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Ropivacaine Other / unclassified 0.375 % —
Background Acetaminophen Small molecule 1000 mg —
Background Bupivacaine Other / unclassified 0.5 % —
Background Ketoprofen Small molecule 100 mg —
Background dipyrone Unknown 1000 mg —

Indications