RecruitingNot Applicable

Quality of Postoperative Analgesia and Functional Recovery After Elective Cesarean Delivery

Switzerland63 participantsStarted 2024-06-12

Plain-language summary

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

Who can participate

Age range18 Years

SexFEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

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: * patients with inability to consent * patient refusal * contraindication to spinal anesthesia (eg, hemodynamic instability, infection at the surgery site, and neurologic defects such as transverse myelitis) * emergency cesarean delivery * preeclampsia/eclampsia * allergy to drugs used in the protocol

What they're measuring

Patient Controlled Analgesia morphine consumption

Timeframe: Day 1 after cesarean section

obstetric quality of recovery score

Timeframe: Day 1 after cesarean section

Trial details

NCT IDNCT06355271

SponsorEnte Ospedaliero Cantonale, Bellinzona

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2027-12-31

Contact for this trial

Roberto Dossi

0918119341 roberto.dossi@eoc.ch

View on ClinicalTrials.gov More Obstetric Pain trials