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Pain Score and Opioid Consumption of Index and Previous Cesarean Delivery

P

Prince of Songkla University

Status

Not yet enrolling

Conditions

Postoperative
Pain

Treatments

Other: No intervention

Study type

Observational

Funder types

Other

Identifiers

NCT06178458
66-348-8-1

Details and patient eligibility

About

Postoperative pain after cesarean delivery is common and affects on both mothers and children.

The goals of this retrospective observational study aim to predict pain score and opioid consumption of index cesarean delivery from pain score and opioid consumption of previous cesarean delivery.

Full description

The authors will review the medical records of recruited participants for demographic data as well as pain scores and opioid consumption of index cesarean delivery and previous cesarean delivery.

Enrollment

416 estimated patients

Sex

Female

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patients who had at least 2 cesarean deliveries
  • Patients received spinal anesthesia and intrathecal morphine for cesarean delivery
  • Patients received postoperative pain control as per standard protocol

Exclusion criteria

  • Patients with chronic pain prior to cesarean delivery
  • Unable to give pain score
  • Receiving general anesthesia for cesarean delivery
  • Receiving postoperative pain control beyond the standard protocol
  • Patients with multiple pregnancy, placenta abruption, placenta accrete, postpartum hemorrhage
  • Patients with psychotic disorder

Trial contacts and locations

0

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Central trial contact

Sasikaan Nimmaanrat, MD, MMed; Boonsin Tangtrakulwanich, MD

Data sourced from clinicaltrials.gov

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