CompletedPhase 4ACTRN12606000506594

Oral analgesia compared with intrathecal morphine for pain after caesarean delivery: a randomised controlled trial

Oral oxycodone analgesia compared with intrathecal morphine for pain relief after caesarean delivery: a randomised controlled trial


Sponsor

Individual (Michael Paech)

Enrollment

120 participants

Start Date

Jan 21, 2007

Study Type

Interventional

Conditions

Summary

This study will investigate two methods of pain relief after caesarean section conducted under regional anaesthesia. Our hypothesis is that multimodal analgesia including intrathecal morphine is more effective than multimodal analgesia with regular administration of oral opioid.


Eligibility

Sex: Both males and femalesMin Age: 18 Yearss

Plain Language Summary

Simplified for easier understanding

This study is looking at: Oral analgesia compared with intrathecal morphine for pain after caesarean delivery: a randomised controlled trial. It is open to Both males and females, aged 18 and older. There are also some health conditions and factors that may prevent you from joining.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

Intervention group: Intrathecal morphine 100 mcg given with spinal anaesthesia immediately preoperatively.

Intervention group: Intrathecal morphine 100 mcg given with spinal anaesthesia immediately preoperatively. Both control group and intervention groups also receiving oral paracetamol 1 g in recovery and 6 hourly until 24 hours postoperatively plus diclofenac 100 mg per rectum at completion of surgery and diclofenac 50 mg orally 8 hourly until 24 hours postoperatively, after caesarean section.


Locations(1)

Australia

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ACTRN12606000506594