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Magnesiumsulphate for Postoperative Analgesia In the Newly delivered, The MAG-PAIN randomized controlled trial.

Status
Not yet recruiting
Phases
Phase 2
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-519617-56-00
Enrollment
150
Registered
2025-03-17
Start date
Unknown
Completion date
Unknown
Last updated
2025-03-17

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

Conditions

Postoperative pain

Brief summary

Acute postoperative pain within 6 hours

Detailed description

Acute postoperative pain after 14 days, in both rest and movement., Acute postoperative pain after 24 hours, in both rest and movement, Persistent postoperative pain after 3 months in both rest and movement., Early recovery after 24 hours, Early recovery after 14 days., Opioidconsumption. Total opioid dose in intravenous morphine milligram equivalents after 24 hours., Postoperative nausea and vomiting. Highest intensity after 24 hours., Self-evaluated quality of breastfeeding and fetal connection. Highest score between 0 and 10 is compared between groups after 24 hours., Self-evaluated quality of breastfeeding and fetal connection. Highest score between 0 and 10 is compared between groups after 14 days.

Interventions

DRUG-
DRUGMAGNESIUM SULFATE

Sponsors

Region Halland
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to 64 Years

Design outcomes

Primary

MeasureTime frame
Acute postoperative pain within 6 hours

Secondary

MeasureTime frame
Acute postoperative pain after 14 days, in both rest and movement., Acute postoperative pain after 24 hours, in both rest and movement, Persistent postoperative pain after 3 months in both rest and movement., Early recovery after 24 hours, Early recovery after 14 days., Opioidconsumption. Total opioid dose in intravenous morphine milligram equivalents after 24 hours., Postoperative nausea and vomiting. Highest intensity after 24 hours., Self-evaluated quality of breastfeeding and fetal connection. Highest score between 0 and 10 is compared between groups after 24 hours., Self-evaluated quality of breastfeeding and fetal connection. Highest score between 0 and 10 is compared between groups after 14 days.

Countries

Sweden

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026