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Comparison of Ultrasound-guided Quadratus Lumborum Block and Iliohypogastric/Ilioinguinal Nerve Block for Postoperative Pain Management in Patients Undergoing Cesarean Section

Not Applicable
Conditions
Cesarean Section
Quadratus Lumborum Block
Iliohypogastric/Ilioinguinal Nerve Block
Registration Number
NCT04822870
Lead Sponsor
Peking University People's Hospital
Brief Summary

The purpose of this study is to compare the analgesic effect of ultrasound-guided quadratus lumborum block and iliohypogastric/ilioinguinal nerve block for postoperative pain management in patients undergoing cesarean section.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
Female
Target Recruitment
87
Inclusion Criteria
  • singleton pregnancy
  • gestation of at least 37 weeks
  • American Society of Anesthesiologists (ASA) physical status I or II
  • finish Pfannenstiel section under combined spinal and epidural anesthesia
Exclusion Criteria
  • pruritus existed before the surgery
  • allergic to lidocaine, ropivacaine or dexamethasone

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
morphine consumption24 hours postoperatively

Every parturient use a patient-controlled intravenous analgesia pump as supplement for the interventions. The analgesia pump contains morphine and can record morphine consumption. Postoperative use of morphine can reflect analgesic effect.

Secondary Outcome Measures
NameTimeMethod
morphine consumption48 hours postoperatively

Every parturient use a patient-controlled intravenous analgesia pump as supplement for the interventions. The analgesia pump contains morphine and can record morphine consumption. Postoperative use of morphine can reflect analgesic effect.

effective analgesia time48 hours postoperatively

Time period between finish the intervention and the first time parturient use the patient-controlled intravenous analgesia pump for analgesia supplement.

satisfaction score48 hours postoperatively

Ask the patient to evaluate satisfaction score using 0-10. 0 refers totally dissatisfied, 10 refers to the most satisfied

hospital stayat discharge assessed up to 10 days

The hospitalize length

pain score48 hours postoperatively

Use visual analogue scale (VAS) 0-10 to evaluate pain intensity and reflect analgesic effect. 0 refers to completely no pain, 10 refers to the most severe pain she has experienced.

adverse effect48 hours postoperatively

Nausea and vomiting, pruritus, oversedation, respiratory depression and urinary retention are considered adverse effects. The incidence and severity are recorded, 1 score refers to mild, 2 scores refers to moderate, 3 scores refers to severe and treatment needed.

hospitalize costat discharge assessed up to 10 days

Total cost in this hospitalization

Trial Locations

Locations (1)

Peking University People's Hospital

🇨🇳

Beijing, Beijing, China

Peking University People's Hospital
🇨🇳Beijing, Beijing, China

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