Trial · NCT02311543
Impact of a Surgical Sealing Patch on Lymphatic Drainage After ALND for Breast Cancer
NCT02311543, Phase 3, Completed, Swiss Cancer Institute
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Impact of a Surgical Sealing Patch on Lymphatic Drainage After ALND for Breast Cancer. Trials, record NCT02311543. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02311543
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Impact of a Surgical Sealing Patch on Lymphatic Drainage After ALND for Breast Cancer
- NCT number
- NCT02311543
- Status
- Completed
- Phases
- Phase 3
- Enrollment
- 142 participants, actual
- Lead sponsor
- Swiss Cancer Institute
- Conditions
- Breast Cancer
- Interventions
- TachoSil® patches
- First posted
- 2014-12-08
- Last updated
- 2019-05-15
Source ClinicalTrials.gov
Registered outcomes7
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Total volume of axillary drainage | until drain removal (2 - 10 days after surgery) | Total volume of axillary drainage in ml until drain removal. |
| Secondary | Volume of axillary drainage per 24 hours | until drain removal (2 - 10 days after surgery) | Volume of axillary drainage per 24 hours in ml will be calculated as the total volume of axillary drainage in ml until drain removal divided by the total duration of axillary drainage in days |
| Secondary | Total duration of axillary drainage in days | until drain removal (2 - 10 days after surgery) | Total duration of axillary drainage in days will be calculated from the date of surgery to the date of axillary drain removal |
| Secondary | Duration of postoperative hospital stay in days | between 3-6 days after surgery | Duration of postoperative hospital stay in days will be calculated from the date of surgery to the date of hospital discharge. |
| Secondary | Patients with clinically relevant seroma | until 24 weeks after surgery | Clinically relevant seroma is defined as either causing discomfort or requiring aspiration. |
| Secondary | Number of clinically relevant seroma aspirations | until 24 weeks after surgery | Number of clinically relevant seroma aspirations until 24 weeks after surgery |
| Secondary | Total volume of all clinically relevant seroma aspirations in ml | until 24 weeks after surgery | Total volume of all clinically relevant seroma aspirations in ml until 24 weeks after surgery |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers1
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as |
|---|---|
| 29948418 | RESULT |
Source PubMed
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT02311543
GET https://conductscience.org/api/trials/v1/NCT02311543/registered