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Bilateral thoracic paravertebral block combined with PCIA for postoperative pain management after upper abdominal surgery: a randomised controlled trial

Bilateral thoracic paravertebral block combined with PCIA for postoperative pain management after upper abdominal surgery: a randomised controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800015790
Enrollment
Unknown
Registered
2018-04-20
Start date
2018-04-18
Completion date
Unknown
Last updated
2018-04-30

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

Conditions

Postoperative Pain

Interventions

PVB :bilateral thoracic paravertebral block
PCA:none

Sponsors

Beijing Friendship Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 80 Years

Inclusion criteria

Inclusion criteria: The patient undergoing elective Whipple or hepatectomy; aged 18 to 75 years old; ASA I - III, BMI15-30 kg/m2; Understand the informed consent and agree to sign the informed consent form before this study

Exclusion criteria

Exclusion criteria: Fail to finish the surgery; reoperation in 3 days after surgery; contraindication to the use of bilateral thoracic paravertebral block; the patient who required to withdrew the study; patients who were lost to follow.

Design outcomes

Primary

MeasureTime frame
VAS score;—

Secondary

MeasureTime frame
BP;Heart rate;SpO2;BIS;Patient Satisfaction;the duration of staying inPACU;The hospital stay;the usage of sufentanil;—

Countries

China

Contacts

Public ContactXiu-liang Li

Department of Anesthesiology, Beijing Friendship Hospital, Capital Medical University

lixiulianglxl@sina.com+86 13661360712

Outcome results

None listed

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