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UnknownNCT03195309

A Comparison of Different Concentration Ropivacaine for Patient-controlled Epidural Analgesia

A Comparison of Different Concentration Ropivacaine Combination With Fentanyl for Patient-controlled Epidural Analgesia After Cesarean Delivery

Status
Unknown
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
120 (estimated)
Sponsor
Kaohsiung Medical University Chung-Ho Memorial Hospital · Academic / Other
Sex
Female
Age
20 Years – 45 Years
Healthy volunteers
Not accepted

Summary

To compare the postoperative analgesic effect and the intensity of motor block in different concentration ropivacaine plus fentanyl when used epidurally with a patient-controlled analgesia device after Cesarean delivery.

Detailed description

1. Written informed consent must be obtained before any study specific procedures are undertaken. 2. All patients were received epidural anesthesia with 2% Lidocaine and patient-controlled epidural analgesia (PCEA) for post- operative pain control. PCEA randomly allocated into three groups. Group A patients received 0.08% ropivacaine plus 4 mcg /mL fentanyl, Group B patients received 0.08% ropivacaine plus 2mcg /mL fentanyl, and Group C patients received 0.16 % ropivacaine plus 2 mcg /mL fentanyl. Dermographic data, dosage of PCEA during first 48 hours post-operation,NRS scores, patient satisfaction and the intensity of motor block will be recorded and analyzed.

Conditions

Interventions

TypeNameDescription
DRUGRopivacaineCompare different concentration of ropivacaine and fentanyl for elective Cesarean delivery post operative pain control.
DRUGFentanylCompare different concentration of ropivacaine and fentanyl for elective Cesarean delivery post operative pain control.

Timeline

Start date
2017-01-20
Primary completion
2018-12-01
Completion
2019-06-01
First posted
2017-06-22
Last updated
2017-06-22

Locations

1 site across 1 country: Taiwan

Source: ClinicalTrials.gov record NCT03195309. Inclusion in this directory is not an endorsement.