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

  • STATUS
    Recruiting
  • End date
    Dec 23, 2022
  • participants needed
    120
  • sponsor
    Paula Diéguez García
Updated on 23 January 2021

Summary

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.

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

Eligibility

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

How to participate?

Step 1 Connect with a site
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer to help accelerate the development of new treatments and to get notified about similar trials.

You are contacting

Investigator Avatar
Name

Primary Contact

site
Name

Phone Email

0/250
Please verify that you are not a bot.

Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

Learn more

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.

Learn more

Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

Learn more

Similar trials to consider

Loading...

Not finding what you're looking for?

Every year hundreds of thousands of volunteers step forward to participate in research. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.

Sign up as volunteer

user name

Added by • 

 • 

Private

Reply by • Private
Loading...

Lorem ipsum dolor sit amet consectetur, adipisicing elit. Ipsa vel nobis alias. Quae eveniet velit voluptate quo doloribus maxime et dicta in sequi, corporis quod. Ea, dolor eius? Dolore, vel!

  The passcode will expire in None.
Loading...

No annotations made yet

Add a private note
  • abc Select a piece of text from the left.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.
Add a private note