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Clinical Trials/NCT03990922
NCT03990922
Completed
Not Applicable

Continuous Thoracic Paravertebral Block for Open Hepatectomy

Cui Xulei1 site in 1 country76 target enrollmentJune 20, 2019

Overview

Phase
Not Applicable
Intervention
Continuous Paravertebral "block" with saline
Conditions
Pain Management
Sponsor
Cui Xulei
Enrollment
76
Locations
1
Primary Endpoint
the postoperative recovery quality on postoperative day 7
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

Moderate to severe postoperative pain often influence patients quality of recovery after hepatectomy. Systemic opioids given with patient-controlled analgesia has been used after hepatectomy in many medical center, but the analgesic effect can be limited and undesirable side effects may bring about negative effects on patients recovery. Regional block has been proved to improve patients postoperative recovery in many kinds of surgeries.

The investigators therefore designed a prospective, randomized, subject and assessor blinded, parallel-group, placebo controlled study to test the hypothesis that continuous right thoracic paravertebral block increase patients quality of recovery score on the 7th postoperative day after hepatectomy in patients receiving i.v. patient-controlled analgesia (PCA) with morphine.

Registry
clinicaltrials.gov
Start Date
June 20, 2019
End Date
November 17, 2019
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Cui Xulei
Responsible Party
Sponsor Investigator
Principal Investigator

Cui Xulei

attending physician

Peking Union Medical College Hospital

Eligibility Criteria

Inclusion Criteria

  • Age 18-70 yrs
  • American Society of Anesthesiologists physical statusⅠ-Ⅲ
  • Undergo hepatectomy with J-shape subcostal incision
  • Informed consent

Exclusion Criteria

  • A known allergy to the drugs being used
  • Coagulopathy, on anticoagulants
  • Analgesics intake, history of substance abuse
  • Participating in the investigation of another experimental agent
  • Inability to properly describe postoperative pain to investigators (eg, language barrier, neuropsychiatric disorder)

Arms & Interventions

CTPVB with saline

Continuous Paravertebral block with saline and Patient-controlled analgesia with morphine

Intervention: Continuous Paravertebral "block" with saline

CTPVB with ropivocaine

Continuous Paravertebral block with ropivacaine and Patient-controlled analgesia with morphine

Intervention: Continuous Paravertebral block with ropivacaine

CTPVB with ropivocaine

Continuous Paravertebral block with ropivacaine and Patient-controlled analgesia with morphine

Intervention: Patient-controlled analgesia with morphine

CTPVB with saline

Continuous Paravertebral block with saline and Patient-controlled analgesia with morphine

Intervention: Patient-controlled analgesia with morphine

Outcomes

Primary Outcomes

the postoperative recovery quality on postoperative day 7

Time Frame: at the 7th postoperative day

The postoperative recovery quality is evaluated with QoR-15 questionnaire. The QoR-15 is a 15-item questionnaire intended to measure QoR after anesthesia and surgery. It comprises five subscales: pain (2 items), physical comfort (5 items), physical independence (2 items), psychological support (2 items), and emotional state (4 items) \[2 Stark PA, Myles PS, Burke JA. Development and psychometric evaluation of a postoperative quality of recovery score: the QoR- 15. Anesthesiology. 2013;118(6):1332.\]. Each item is scored from 0 to 10, and the possible total score ranges from 0(extremely poor quality of recovery) to 150 (excellent quality of re covery).

Secondary Outcomes

  • post operative length of stay(Up to 2 weeks)
  • time to resumption of bowel movement(Up to 2 weeks after surgery)
  • the postoperative recovery quality on postoperative day 3(at the 3th postoperative day)
  • The pain scores determined by the numeric rating scale (NRS, 0-10)(At 8, 24,48 hours after the surgery)
  • cumulated morphine consumption(At 8, 24,48 hours after the surgery)
  • time to out-of bed activity/ambutation(Up to 2 weeks)

Study Sites (1)

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