Quality of Postoperative Analgesia and Functional Recovery After Elective Cesarean Delivery
Recruiting
N/A
Interventional Study
Obstetric Pain
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Female
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 63 (estimated)
- Sponsor
- Ente Ospedaliero Cantonale, Bellinzona · Other
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About This Trial
Based on randomization, patients will receive a mixture for spinal anesthesia and will be followed in the following hours for the various outcomes and for functional recovery
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* patients over 18 year of age
* height over 160 cm
* American Society Anesthesiologists physical status I and II
* term singleton parturients
* scheduled for elective cesarean delivery during spinal anesthesia at Ospedale Regionale Bellinzona Valli
Exclusion Criteria:
* patie…
Contacts