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Magnesium as Adjuvant for Sciatic Block (Mg)

C

Campus Bio-Medico University of Rome

Status

Completed

Conditions

Hallux Valgus

Treatments

Drug: Ropivacaine
Drug: Magnesium Sulfate

Study type

Interventional

Funder types

Other

Identifiers

NCT02198547
CarGalMg

Details and patient eligibility

About

The aim of the study is to evaluate if Magnesium added to ropivacaine can reduce onset time and can enhance offset time.

Full description

Patients are randomly divided into two groups: group "M" (Ropivacaina 7,5 mg/ml with Mg 4 mg/Kg)and group"C" (without Mg).

Standard monitoring is applied to each patient in perioperative period. An indipendent observer collect data: time to perform block, sensitivity onset,motor onset, pain during surgery and complication.

In the post-operative period till 24 hours for each patient is evaluated off-set time, pain and analgesic consumption.

Enrollment

60 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • given consent
  • allux valgus correction surgery

Exclusion criteria

  • allergy to local anesthetic
  • infection in the site of puncture

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

60 participants in 2 patient groups

Ropivacaine Magnesium sulfate
Experimental group
Description:
Locoregional anesthesia for valgus allux correction with ropivacaine 7,5 mg/ml and Mg 4 mg/Kg. Sciatic block at popliteal level.
Treatment:
Drug: Magnesium Sulfate
Ropivacaine
Active Comparator group
Description:
Patients undergoing allux valgus correction with locoregional anesthesia with ropivacaine 7,5 mg/ml, without MG
Treatment:
Drug: Ropivacaine

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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