Skip to content

Ultrasound-Guided Erector Spinae Plane Block Versus Thoracic Paravertebral Block on Postoperative Analgesia After Laparoscopic Nephroureterectomy: a Study Protocol from a Non-inferiority, Double Blinded RCT

Ultrasound-Guided Erector Spinae Plane Block Versus Thoracic Paravertebral Block on Postoperative Analgesia After Laparoscopic Nephroureterectomy: a Study Protocol from a Non-inferiority, Double Blinded RCT

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000031916
Enrollment
Unknown
Registered
2020-04-14
Start date
2020-04-15
Completion date
Unknown
Last updated
2021-01-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

perioperative regional anesthesia and analgesia

Interventions

Sponsors

Peking University First Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Participants meet all of the following criteria will be enrolled in this study: (1) Age between 18 and 75 years; (2) Plan to undergo LRNU; (3) Agree to receive regional nerve block and postoperative intravenous controlled analgesia (PCIA); (4) American Society of Anesthesiologist physical status Classification I-III; (5) Agree to participate in the study and signed the informed consent.

Exclusion criteria

Exclusion criteria: (1) BMI > 35kg/m2 or 442µmol/L or requirement of renal replacement therapy), liver dysfunction (Child-Pugh Class C) and heart failure; (3) Contraindication of deep nerve block, including but not limited to be allergic to anesthetic drug, coagulation disorder, infection at the injection site; (4) Chronic opioids dependence and long-term use of various analgesics for chronic pain over 3 months; (5) Unable to communicate preoperatively due to severe dementia, language barrier or neuropsychiatric disorder, or else; (6) Unable to perform nerve block procedure due to difficult anatomy through ultrasound scan.

Design outcomes

Primary

MeasureTime frame
a joint endpoint of cumulative 24h opioids consumption after surgery and average pain NRS score at 24th h (valued the average from NRS at rest and with movement at 24th h) postoperatively.;

Secondary

MeasureTime frame
cumulative opioids consumption at different time (0.5h, 2h, 6h, 18h, 24h and 48h) after surgery;somatic and visceral NRSpain scores both at rest and with movement at 0.5th h, 2nd h, 6th h, 18th h, 24th h, 48th h postoperatively;the time interval to the first bolus demand in PCIA pump;the numbers of required boluses in PCIA pump;the numbers of administered boluses in PCIA pump;the numbers of rescue analgesia besides PCIA pump;

Countries

China

Contacts

Public ContactHong Zhang

Peking University First Hospital

zhanghong40@hotmail.com+86 13910104660

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026