Trials / Completed
CompletedNCT03990922
CTPVB for Hepatectomy
Continuous Thoracic Paravertebral Block for Open Hepatectomy
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 76 (actual)
- Sponsor
- Cui Xulei · Academic / Other
- Sex
- All
- Age
- 18 Years – 70 Years
- Healthy volunteers
- Not accepted
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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Continuous Paravertebral block with ropivacaine | Inject 25 ml 0.5% ropivacaine in the T8 paravertebral space followed with catheter insertion and continuous 0.2% ropivacaine infusion(infusion rate: 0.125ml/kg/pulse,1pulse/h). |
| PROCEDURE | Continuous Paravertebral "block" with saline | Inject 25 ml 0.9% saline in the T8 paravertebral space followed with catheter insertion and continuous 0.9% ropivacaine infusion(infusion rate: 0.125ml/kg/pulse,1pulse/h). |
| DRUG | Patient-controlled analgesia with morphine | Morphine given as intravenous patient-controlled analgesia bolus: 2mg, lock time: 5min, 1h limitation: 8mg |
Timeline
- Start date
- 2019-06-20
- Primary completion
- 2019-11-09
- Completion
- 2019-11-17
- First posted
- 2019-06-19
- Last updated
- 2020-01-02
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT03990922. Inclusion in this directory is not an endorsement.