KCT0009420RecruitingUnknown
Patient-driven compression versus non-compression Strategy after endovenous thermal ablation for chronic venous disease
Jeju Soo Cardio-Vascular Clinic0 sites406 target enrollmentStarted: TBDLast updated:
Trial Snapshot
- Phase
- Unknown
- Status
- Recruiting
- Sponsor
- Enrollment
- 406
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Observational
Eligibility Criteria
- Ages
- 18(Year) to 64(Year) (—)
- Sex
- All
Inclusion Criteria
- •Individuals who have undergone Endothermal Ablation for unilateral or bilateral lower limbs with Chronic Venous Disease (CVD) and voluntarily consent to participate in this study.
- •Individuals aged 18 to less than 65, capable of making independent and voluntary decisions.
- •Patients with clinical stage C2 in both lower limbs: Definition of C2 includes 1) External varix (protruding varicose veins) or 2) Vessels where reflux is observed with a diameter of 3.0mm or more.
Exclusion Criteria
- •Patients under 18 years old or above 65 years old (with potential limitations in autonomous and voluntary decision-making).
- •Foreign patients with communication difficulties.
- •Patients for whom follow-up observations are not feasible.
- •Patients with a d-dimer level of 0.5 or higher in preoperative blood tests and those taking aspirin for anticoagulation purposes before and after the procedure.
- •Patients with Peripheral Arterial Occlusive Disease (PAOD) corresponding to ABI<0.6.
- •Patients with clinical stage C4 or higher on one side or both sides.
- •Patients continuously using analgesics for pain control due to other medical conditions (e.g., rheumatoid arthritis).
- •Individuals with previous experience of wearing medical compression stockings.
Investigators
Similar Trials
Recruiting
Not Applicable
Effect of patient-specific compression aids based on 3D printing for hypertrophic burn scar on faceDiseases of the skin and subcutaneous tissueKCT0005918Hallym University Medical Center-Hangang44
Completed
Unknown
Controlled decompression effects in the patients with severe TBI: A Randomized Control TrialIRCT20230907059376N1Afridi Medical Complex, Peshawar52
Completed
Not Applicable
Effectiveness of chest compression for patients with out-of-hospital cardiac arrestout-of-hospital cardiac arrestJPRN-UMIN000007933Sapporo Fire Bureau400
Recruiting
Not Applicable
Carepace compression system compared to standard postoperative threatment after pacemaker or defibrillator implantT81.0T82.1Haemorrhage and haematoma complicating a procedure, not elsewhere classifiedMechanical complication of cardiac electronic deviceDRKS00009808Medizinische Klinik m. S. Kardiologie Rhythmologie-Elektrophysiologie und Devicetherapie; Charité Campus Virchow Klinikum120
Completed
Phase 3
Evaluation of the effect of compression therapy by using surgical gloves on nab-paclitaxel-induced peripheral neuropathy in primary breast cancer patients:a phase 3 multicenter study (single-armed study)Breast cancerJPRN-UMIN000024836Kamigata Breast Cancer Study Group61
