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Clinical Trial Summary

The purpose of this study is to investigate the effect of different kinds of popular peripheral nerve blocks for postoperative analgesia after cesarean delivery is completed, compared with traditional epidual analgesia.


Clinical Trial Description

Visual Analogue Scale (VAS) and morphine consumption was adopted to evaluate the pain relief. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03333902
Study type Interventional
Source First Affiliated Hospital, Sun Yat-Sen University
Contact
Status Completed
Phase N/A
Start date December 1, 2017
Completion date August 30, 2018

See also
  Status Clinical Trial Phase
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Completed NCT05099055 - Dexmedetomine as Adjuvant for Spinal Anesthesia in Elective Cesarian Sections : a Pilot Study Phase 3
Completed NCT02958215 - Phenylephrine and Hypotension During Spinal Anesthesia for Cesarean Section Phase 2
Active, not recruiting NCT03167905 - CODEPAD (Collaborative Outcomes of DEpression and Pain Associated With Delivery) Phase 2/Phase 3
Recruiting NCT03164096 - The Effect of Some Parturients' Characteristics on Sensory Block Level After Spinal Anesthesia Phase 4
Completed NCT05091294 - The Effect of Injection Rate of Local Anesthetic in Caesarean Section N/A
Completed NCT04205344 - Subarachnoid Bupivacaine in Obese Patients Undergoing Cesarean Delivery Phase 4