Clinical Trials Directory

Trials / Terminated

TerminatedNCT03791736

Evaluation of Impact of Sandostatin® Injection Before Axillary Clearance on Lymphocele Formation

Evaluation of Impact of Sandostatin® Injection Before Axillary Clearance on Lymphocele Formation In Patients With Breast Cancer

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
4 (actual)
Sponsor
Institut Cancerologie de l'Ouest · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

The lymphocele is the main early postoperative complication of axillary clearance for breast cancer patients with rates up to 85%. The usual treatment consists of external drainage. However, this method increases the duration of hospitalization. As a result, some practitioners have abandoned drainage, allowing for ambulatory surgery. If this solution makes it possible to reduce the duration of the hospitalizations, it involves iterative punctures of the axillary hollow in case of lymphocele These punctures may be responsible for pain, hematoma or infection of the operative site. To date, no method has proved superior in terms of decreasing the incidence of lymphocele postoperatively axillary clearance. Octreotide (Sandostatin®) is a peptide, one of whose effects is to reduce the inflammation responsible for lymphoceles. The aim of the study is to inject Sandostatin® before surgery, with the aim of reducing the incidence of seroma by 50% after axillary clearance

Conditions

Interventions

TypeNameDescription
PROCEDUREInjection of sandostatineIntramuscular injection of sandostatin 30 mg 3 days before surgery

Timeline

Start date
2016-07-06
Primary completion
2018-07-06
Completion
2018-07-06
First posted
2019-01-03
Last updated
2022-07-28

Source: ClinicalTrials.gov record NCT03791736. Inclusion in this directory is not an endorsement.