Intercostal Nerves Block in the Midaxillary Line Versus Paravertebral Block for no Reconstructive Breast Surgery

  • End date
    Dec 23, 2022
  • participants needed
  • sponsor
    Paula Diéguez García
Updated on 23 January 2021


The main objectives of the trial are the efficacy and safety of intercostal nerve block in the midaxillary line versus paravertebral block, both guided by ultrasound in patients scheduled for not reconstructive breast surgery.

Condition no Reconstructive Breast Surgery
Treatment Paracetamol, paravertebral block, BRILMA, dexketoprofen
Clinical Study IdentifierNCT02018601
SponsorPaula Diéguez García
Last Modified on23 January 2021


Yes No Not Sure

Inclusion Criteria

Is your age between 18 yrs and 75 yrs?
Are you female?
Do you have no Reconstructive Breast Surgery?
Do you have any of these conditions: Do you have no Reconstructive Breast Surgery??
Patients scheduled for not reconstructive unilateral breast surgery
Physical status American Society Anesthesiologists (ASA) I-III
Signed informed consent
Aged between 18 and 75 years
Ability to assess pain using a verbal and numerical scales
Assessment of pain at the time of inclusion in the study is lower than 3 verbal simple scale

Exclusion Criteria

Personal history of disorders of hemostasis or previous history of abnormal bleeding evidence
Local infection at the site of the puncture or to puncture prior systemic
Contraindications to study medication
Muscle or neurological disease, peripheral or central
Patients with prior history of opioid
Pregnancy or lactation
Difficulties in assessing pain or inability to understand or assist in the development of the study (psychiatric illness, cognitive impairments)
Active Chronic alcoholism or drug addiction
BMI under 20 or mayor 30
Chronic treatment with non-steroidal anti-inflammatory drugs, antidepressants, anticonvulsants or opioids
Rejection of the patient
Clear my responses

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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