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
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Injection of sandostatine | Intramuscular 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.