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Postoperative Pain Management of Caesarean Section

Postoperative Pain Management of Caesarean Section: a Prospective, Observational Cohort Study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05009771
Enrollment
100
Registered
2021-08-18
Start date
2022-02-23
Completion date
2026-07-31
Last updated
2025-05-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Analgesia, Caesarean Section, Postoperative Pain

Keywords

Postoperative Pain, Caesarean section, Postpartum rehabilitation, Dinalbuphine sebacate, PCA, NALDEBAIN

Brief summary

Caesarean section is one of the most frequent surgeries causing severe postoperative pain. Poor management of acute pain can contribute to postoperative complications, late recovery and the development of chronic pain. Moreover, it had been demonstrated that the intensity of postpartum pain is associated with depression. It is imperative to find out appropriate methods of postpartum pain alleviation. Currently, a lot of analgesic drugs and methods have been developed and used in clinical practice, such as patient-controlled analgesia, extended-release analgesics and multimodal analgesia. This prospective cohort study is aimed to investigate the outcome of each postoperative analgesic method used in caesarean section.

Detailed description

This is a prospective, observational, cohort study. Patients undergoing elective caesarean section will be invited to the study. The written informed consent will be obtained prior to participation. After getting the written informed consent, data will be collected from medical records, questionnaires, patient diaries, visit records and telephone visit records. Through telephone visits, postpartum depression scale and postpartum chronic pain will be evaluated six weeks and three months after delivery. Demographic data, consumption of analgesics, analgesic methods, intensity of postoperative pain, complications, recovery time, score of depression scale will all be summarized. Numerical variables will be present with mean and standard deviation and categorical variables will be present with number and percentage.

Interventions

DRUGIntravenous patient-control analgesia

At the two trial sites, IV-PCA is commonly used with morphine. The device is installed after delivery and removed within 3 days.

Dinalbuphine sebacate is a prodrug of nalbuphine. With oil-based formulation, the active ingredient releases slowly and the effect lasts longer than nalbuphine. After delivery, a single 150 mg dose of dinalbuphine sebacate is administered intramuscularly.

Sponsors

Mackay Memorial Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

1. Aged 20 to 40. 2. Planing to undergo caesarean section with spinal anesthesia. 3. Scheduled to undergo cesarean section between 37 and 40 weeks of gestation. 4. American Society of Anesthesiology Physical Class 1-2. 5. Planing to alleviate postoperative pain with intravenous patient-controlled analgesia or administration of NALDEBAIN.

Exclusion criteria

1. Not willing to provide informed consent. 2. Unable to receive opioids or NSAIDs due to contraindication. 3. Long-term use of opioids or drug abuse. 4. Suffering from chronic pain disease. 5. Having medical history of mental illnesses. 6. Diagnosed with Pre-eclampsia or eclampsia. 7. Diagnosed with gestational diabetes. 8. Unsuitable for participation judged by investigator.

Design outcomes

Primary

MeasureTime frameDescription
Postpartum pain intensityWithin 5 days after deliveryPain intensity is assessed by numerical rating scale (NRS) at least twice daily during hospital stay after delivery. NRS is a 11-point scale which labeled from zero (no pain) to ten (worst pain). The area under the curve of NRS are calculated.

Secondary

MeasureTime frameDescription
Incidence of complicationsUp to 5 days after deliverythe incidence of postoperative complication occurring during hospital stay after delivery, especially the ones related to analgesics.
AmbulationUp to 5 days after deliveryThe mean length of time between delivery and the first ambulation.
BreastfeedingUp to 5 days after deliveryThe percentage of participants able to breastfeed during hospital stay and the mean length of time between delivery and the first breastfeeding.
Consumption of analgesicsWithin 5 days after deliveryThe mean total consumption of analgesics during the hospital stay after delivery.
Postnatal Depression assessmentAt baseline, 6 weeks and 3 months after deliveryEdinburgh Postnatal Depression questionnaire is used to assess patients' postpartum depression. Participants are asked to fill in the questionnaire at baseline (within 30 days prior to delivery), 6 weeks and 3 months after delivery.
Satisfaction assessed by a four-point scale6 weeks after deliveryParticipants are asked to assess the satisfaction toward rate of recovery progress and pain management through 6 questions six weeks after delivery. Each question contain 4 choices: very satisfied, satisfied, dissatisfied and very dissatisfied.
Chronic pain intensity6 weeks and 3 months after deliveryChronic pain intensity is assessed by NRS 6 weeks and 3 months after delivery. NRS is a 11-point scale which labeled from zero (no pain) to ten (worst pain).
Gastrointestinal function recoveryUp to 5 days after deliveryThe mean length of time between delivery and first soft diet.

Countries

Taiwan

Contacts

Primary ContactChi-Hsu Wang, M.D.
s871017@gmail.com+886-2-2809-4661

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 1, 2026