Supermicrosurgical Lymphvenous Bypass Intervention for Treatment
NCT ID: NCT05270629
Last Updated: 2022-03-08
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
87 participants
OBSERVATIONAL
2021-09-06
2022-09-05
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Endothelial Function in Lower Extremity Bypass Grafts
NCT00759707
Preservation of Venous Valvular Function After PMT for Acute DVT
NCT05588284
A Long Term Follow-up Study of AMG0001 in Subjects With Critical Limb Ischemia
NCT02974179
The eSVS® Mesh Randomized Post-Market Study
NCT01462721
Evaluation of Combination Therapy for Upper Extremity Lymphedema
NCT05825157
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_CONTROL
RETROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Lower limb lymphedema patients
This was a retrospective cohort propensity score-matched study. Patients with lower limb lymphedema were enrolled.
Antegrade and retrograde anastomoses
Patients who had received both antegrade and retrograde anastomoses.
Antegrade-only anastomoses
Patients who had received antegrade-only anastomoses.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Antegrade and retrograde anastomoses
Patients who had received both antegrade and retrograde anastomoses.
Antegrade-only anastomoses
Patients who had received antegrade-only anastomoses.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
18 Years
100 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Chang Gung Memorial Hospital
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Kaohsiung Chang Gung Memorial Hospital
Kaohsiung City, , Taiwan
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
202101384B0
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.