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Adductor Canal Block: Continuous Infusion Versus Automatic Intermittent Bolus

A

ASST Gaetano Pini-CTO

Status

Completed

Conditions

Injury of Anterior Cruciate Ligament

Treatments

Procedure: Automatic Intermittent Bolus of ropivacaine 0.2%
Procedure: Continuous Infusion of ropivacaine 0.2%

Study type

Interventional

Funder types

Other

Identifiers

NCT02589288
IOGPGC09

Details and patient eligibility

About

The aim of this prospective, randomized , blinded study is to compare two different infusion techniques (continuous VS intermittent automatic bolus) to assess the effects of postoperative analgesia after Day-Case anterior cruciate ligament (ACL) reconstruction.

Enrollment

80 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age above 18 years old
  • American society of anesthesiology (ASA) physical status I-II
  • Signed informed consensus

Exclusion criteria

  • ASA >II
  • Unstable neurological disease
  • Diabetic mellitus (DM) type I-II
  • Allergy to used drugs
  • Opioid chronic treatment
  • Consensus refusal or not valid
  • Anticoagulant therapy
  • Postoperative intensive care required

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

80 participants in 2 patient groups

Continuous Infusion
Active Comparator group
Description:
Patients receive a postoperative continuous infusion of Ropivacaine 0,2% at 6 ml/h and 4 ml PCA bolus, lockout 20 minutes via electronic infusion pump (Micrel device, Greece).
Treatment:
Procedure: Continuous Infusion of ropivacaine 0.2%
Automatic Intermittent Bolus
Experimental group
Description:
Patients receive a postoperative Automatic Intermittent Bolus of 6 ml Ropivacaine 0,2% and 4 ml PCA bolus, lockout 20 minutes every hour via electronic infusion pump (Micrel device, Greece).
Treatment:
Procedure: Automatic Intermittent Bolus of ropivacaine 0.2%

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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