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NCT06178458 Clinical Trial

Pain Score and Opioid Consumption of Index and Previous Cesarean Delivery

Pain Clinical Trial

Official title:
Prediction of Pain Score and Opioid Consumption of Index Cesarean Delivery From Pain Score and Opioid Consumption of Previous Cesarean Delivery: A Retrospective Study

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT06178458
Other study ID # 66-348-8-1
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date January 2024
Est. completion date December 2025

Study information
Verified date December 2023
Source Prince of Songkla University
Contact Sasikaan Nimmaanrat, MD, MMed
Phone +66887907842
Email snimmaanrat@yahoo.com.au
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.

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.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 416
Est. completion date December 2025
Est. primary completion date December 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years and older
Eligibility 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

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• No intervention
To collect data of pain score and opioid consumption of index and previous cesarean delivery

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Prince of Songkla University

Outcome
Type Measure Description Time frame Safety issue
Primary Prediction of pain score after cesarean delivery To predict pain score of index cesarean delivery from previous cesarean delivery using pain score measured by verbal numerical rating scale (VNRS) ranging from 0 (no pain) to 10 (worst pain imaginable). January 2024 - December 2025
Secondary Prediction of opioid consumption after cesarean delivery To predict opioid consumption of index cesarean delivery from previous cesarean delivery based on 1. number and percentage of patients who required opioid for controlling postoperative pain, 2. MME (milligram morphine equivalent) per total patients and 3. MME per patients who received opioid January 2024 - December 2025
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