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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 31 August 2015
Main ID:  NCT02527577
Date of registration: 14/08/2015
Prospective Registration: No
Primary sponsor: Centre Hospitalier Universitaire de Saint Etienne
Public title: Analgesia by Transversus Abdominis Plane Nerve Block in Patients Undergoing Liver Resection. BLOC-TAP
Scientific title: Analgesia by Transversus Abdominis Plane Nerve Block in Patients Undergoing Liver Resection
Date of first enrolment: April 2010
Target sample size: 39
Recruitment status: Terminated
URL:  https://clinicaltrials.gov/show/NCT02527577
Study type:  Interventional
Study design:  Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment  
Phase:  N/A
Countries of recruitment
France
Contacts
Name:     carine.labruyere@chu-st-etienne.fr MOLLIEX, MD PhD
Address: 
Telephone:
Email:
Affiliation:  CHU de SAINT-ETIENNE
Key inclusion & exclusion criteria

Inclusion Criteria:

- hepatectomy or segmentectomy

Exclusion Criteria:

- Sepsis uncontrolled current

- Overdose in anticoagulant during general anesthesia

- Thrombocytopenia <50 g / dl

- Severe renal impairment: Cockcroft <30 ml / min

- history of ventricular arrhythmia serious unexplained .*

- Allergy to local anesthetics of the amide

- Contraindication to remifentanil and morphine

- Hypovolemia



Age minimum: 18 Years
Age maximum: N/A
Gender: Both
Health Condition(s) or Problem(s) studied
Liver Cancer, Adult
Intervention(s)
Drug: Placebo
Drug: RopivacaIne chlorhydrate
Primary Outcome(s)
consumption of morphine over the first 48 hours postoperative. [Time Frame: at 48 hours postoperative]
Secondary Outcome(s)
pharmacokinetic of ropivacaine (plasma concentrations) [Time Frame: 1, 2, 3, 6, 10, 24, 36, 48 hours post-dose]
Secondary ID(s)
0908127
2009-017768-18
A100140-28
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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