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Recruiting NCT06355271

NCT06355271 Quality of Postoperative Analgesia and Functional Recovery After Elective Cesarean Delivery

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Clinical Trial Summary
NCT ID NCT06355271
Status Recruiting
Phase
Sponsor Ente Ospedaliero Cantonale, Bellinzona
Condition Obstetric Pain
Study Type INTERVENTIONAL
Enrollment 63 participants
Start Date 2024-06-12
Primary Completion 2027-12-31

Eligibility & Interventions

Sex Female only
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Fentanyl 1Fentanyl2Fentanyl 3

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 63 participants in total. It began in 2024-06-12 with a primary completion date of 2027-12-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief 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

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: * 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

Contact & Investigator

Central Contact

Roberto Dossi

✉ roberto.dossi@eoc.ch

📞 0918119341

Frequently Asked Questions

Who can join the NCT06355271 clinical trial?

This trial is open to female participants only, aged 18 Years or older, studying Obstetric Pain. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06355271 currently recruiting?

Yes, NCT06355271 is actively recruiting participants. Contact the research team at roberto.dossi@eoc.ch for enrollment information.

Where is the NCT06355271 trial being conducted?

This trial is being conducted at Bellinzona, Switzerland.

Who is sponsoring the NCT06355271 clinical trial?

NCT06355271 is sponsored by Ente Ospedaliero Cantonale, Bellinzona. The trial plans to enroll 63 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: September 2026  ·  Data Methodology