SYF74fff93d5935492b9a5a6771f6bb94deRegistry ID: 2024-511010-21-00|RecruitingPhase 4
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interventional
N/A
1 country
1
To prevent the development of chronic postoperative pain after inguinal hernia surgery and knee replacement surgery and to further explore the mechanism behind the development of chronic postoperative pain
Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.
Not reported
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Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.
July 9, 2024
Actual (reported)The effect of Tapentadol compared to placebo on the development of chronic pain in the first year after surgery in patients planned for elective inguinal hernia surgery and knee replacement surgery.
These entries preserve how the registry describes the intervention. Their treatment roles are shown separately from molecular identities.
Formulated product
PALEXIA Retard 50 mg tabletten met verlengde afgifte
The registry describes a specific formulation. Its exact chemical ingredients and approval status require separate evidence.
PROLONGED-RELEASE TABLET
View registry recordThe registry names these ingredients. The formulation’s exact chemical form has not been confirmed.
PALEXIA Retard 50 mg tabletten met verlengde afgifte
Named ingredient: Tapentadol hydrochloride
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Reinier de Graaf Groep
Delft, 2625 AD, Netherlands
Monique van Velzen
First Submitted
July 9, 2024
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Source: European Medicines Agency (EMA), Clinical Trials Information System (CTIS). Original record and public documents are available on CTIS.
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Source retrieved:
Comparison of Postoperative Analgesia Between Intravenous Paracetamol and Intranasal Tapentadol
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