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This clip runs for 21 minutes and was first released on November 18, It starts off slowly with the introduction, from the camera man, of the three lovely ladies while they adopt various poses. I liked the sequence in which the ladies measure their newly swollen busts.

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Select two study versions to compare. Select a version's Submitted Date link to see a rendering of the study for that version. Realization of Pecs blocks 1 and 2 : the patient is in supine position with placing the upper limb in abduction position, a mm needle is inserted under ultrasound using a linear US probe of high frequency after sheathing.

The pectoral nerve block is an innovative technique of locoregional anesthesia that has already been successfully used in breast surgery. Prosthetic breast surgery Locoregional anesthesia Pectoral nerve block Pain Postoperative analgesia. Maximal value of pain intensity according to the numerical scale within the six first hours [ Time Frame: up to First six postoperative hours ]. The investigators hypothesized that the "Pecs blocks 1 and 2" will provide a decrease of the maximal pain of the first 6 post-operative hours after prosthetic breast expansion.

After the anesthesic induction, the interventional team composed by at least a senior anaesthesiologist and a nurse anesthestic, will survey the patient and perform the Pecs blocks, whereas the anesthetic team is outside the room. Pregnant or breast-feeding women according to French law.

Detailed Description: The investigators hypothesized that the "Pecs blocks 1 and 2" will provide a decrease of the maximal pain of the first 6 post-operative hours after prosthetic breast expansion. An intervention team which will be different from the anesthesic teamwill be alone with the patient for 15 minutes, and will realize or not the Pecs blocks according to the randomisation so that all caregivers taking in charge the patients as well as research observers will be blinded.

Click "Compare" to do the comparison and show the differences. In the other group, sterilization, sheating and US are performed but the needle is not inserted.

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Study additions are displayed in green. Study edits or deletions are displayed in red. The interest of this technique has never been assessed in esthetic breast surgery. Outcome Measures Primary Outcome Measures: 1. Maximal value of the pain at day 1 and until day 5 [ Time Frame: Five days ] Value of pain according to a Numeric scalerecorded at day 1 in the hospital, and until day five by phone interview.

The Side-by-Side format only applies to the Protocol section of the study. The pain will be assessed according to a numerical scale. November 17, April 6, November 2, May 14, July 9, Study Status Record Verification:.

Study Description Brief Summary:. The aim of this study is to evaluate the analgesic efficacy of the association of " Pecs blocks 1 and 2 " on pain intensity after breast augmentation surgery.

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One each from columns A and B. Choose either the "Merged" or "Side-by-Side" comparison format to specify how the two study versions are to be displayed. Severe coagulopathy. Vulnerable people. Its realization is fast, simple, and it would be superior compared with a paravertebral block within the framework of mastectomy.

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Hover over the " Recruitment Status " to see how the study's recruitment status changed. Exclusion Criteria: Protected minor or major patients or in the incapacity to give his consent according to the article L of the Code of the Health Public.

Latest version submitted July 9, on ClinicalTrials. Patients participating in another research Allergy with local anesthetics.

Inclusion Criteria: Affiliated to a national insurance scheme Having ed the informed consent for this study Score of American Society of Anesthesiology ASA Be hospitalized in the ambulatory care unit UCA or plastic surgery service for a scheduled esthetic prosthetic breast expansion surgery. A multimodal analgesia, based on the recommendations is proposed to the patients.

Scroll up to access the controls Scroll to the Study top. Maximal value of pain intensity according to the numerical scale within the six first hours [ Time Frame: up to First six postoperative hours ] Secondary Outcome Measures: 1.

Eligibility Minimum Age:. The rest of the anesthesic and surgical care will be identical. Drug: Ropivacaine after dilution with sodium chloride 0. Scroll up to access the controls. References Citations:.

FDA-regulated Drug:. Chronic painful Patients long-term treatment by analgesics Contraindication to use analgesics of the protocol.

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Outcome Measures Primary Outcome Measures:. A study version is represented by a row in the table. Oversight U. FDA-regulated Drug: U. Study Description Brief Summary: Breast augmentation is among the most popular surgical procedures performed in the world with approximately 1, performed in This surgical intervention generates important pains during postsurgical recovery. Breast augmentation is among the most popular surgical procedures performed in the world with approximately 1, performed in Conditions Conditions:.

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This prospective, randomized, double blind study will include 80 patients successively during two years, randomized into two arms : Pecs group and Control group, which will respectively have the block, and no block. Study De Study Type:. National Library of Medicine U. National Institutes of Health U. February 12, None earliest Version on record 2. A yellow table row indicates the study version currently being viewed.

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Breast Cancer Research volume 18Article : 19 Cite this article.

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Breast size is determined by a combination of genetics, lifestyle, and body weight.

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Methods: Magnetic resonance angiography of the abdomen and pelvis at 1.

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Background: Breast augmentation with fat transfer does not bear the risks associated with silicone implantation.

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Background: AeroForm is a new type of remote-controlled, needle-free, carbon dioxide-based expander involving a potentially faster method of tissue expansion.