Post-cesarean Analgesia: Comparing Effectiveness of Staggered v. Simultaneous Therapies

Trial statusRecruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexFemale
Age16+
SponsorThomas Jefferson University

About this trial

Cesarean delivery is a commonly performed surgical procedure associated with worse postpartum pain when compared to vaginal birth. Uncontrolled postpartum pain is associated with increased neonatal and maternal risks. Multimodal non-opioid pain medications, including acetaminophen and non-steroidal anti-inflammatory drugs (NSAIDs) are the preferred first-line therapies. There is no standard practice, however, on best dosing schedules (ie staggered or different time v. simultaneous or same time). This protocol describes a randomized clinical trial aimed to determine whether staggered dosing of acetaminophen and NSAIDs in superior to simultaneous dosing in controlling post-cesarean pain.

Eligibility criteria

Qualifiers

>/= 34 weeks gestation

Singleton pregnancy

Delivery via cesarean section under regional anesthesia

Disqualifiers

Contraindication to acetaminophen or NSAIDs

Current or history of opioid use or misuse

Intrauterine fetal demise

Major congenital anomaly

Trial design

Treatments tested in this trial

  • Acetaminophen
  • NSAID (Ketorolac/Ibuprofen)

Treatment groups

825 Participants
are divided into 2 treatment groups

Sponsors and collaborators