Quality of Life and Health Perception After Surgery of Varicose Veins
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Study Type
Study Type
Enrollment (Actual)
Enrollment
Contacts and Locations
Study Locations
-
-
-
Valladolid, Spain
- Hospital Clinico Universitario de Valladolid
-
-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- patients with reflux in saphenous vein
Exclusion Criteria:
- no reflux in saphenous vein
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
changes in qol questionarie SF-12 after surgery of varicose veins
Time Frame: before and 90 days after surgery
|
measured in SF-12 score
|
before and 90 days after surgery
|
|
changes in qol questionarie Veines QoL/Sym after surgery of
Time Frame: before and 90 days after surgery
|
measured in Veines Qol/Sym score
|
before and 90 days after surgery
|
Secondary Outcome Measures
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
changes in VCSS after surgery of varicose veins
Time Frame: before and 90 days after surgery
|
measured in VCSS score
|
before and 90 days after surgery
|
Collaborators and Investigators
Sponsor
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Study Start
Primary Completion (Actual)
Primary Completion
Study Completion (Actual)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Estimated)
First Posted
Study Record Updates
Last Update Posted (Estimated)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
Other Study ID Numbers
- PI-23-3017
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Quality of Life
-
NCT07378215RecruitingQuality of Life | Postoperative Quality of Recovery | Health-Related Quality-of-Life
-
NCT04239183UnknownQuality of Life of Colostomized Patient
-
NCT02901639UnknownImproving Quality of Life
-
NCT04761367CompletedImprove Quality of Life
-
NCT05722249CompletedProfessional Quality of Life
-
NCT06014671CompletedBreif Description: Patients' Quality of Life of
-
NCT01784497CompletedHealth Related Quality of Life
-
NCT01269489UnknownHealth-related Quality of Life
-
NCT01247636CompletedHealth-Related Quality of Life
Clinical Trials on surgery of varicose veins
-
NCT04436549UnknownVaricose Veins | Symptoms and Signs | Pathology
-
NCT01901731UnknownVaricose Veins | Venous Reflux
-
NCT07163312Not yet recruitingKnee Osteoarthritis | Varicose Veins of Lower Limb | Knee Pain Chronic | Chronic Venous Insufficiency, CVI
-
NCT04115137UnknownObservational Study | Pelvic Congestion Syndrome | Embolization, Therapeutic | Pelvic Varicose Veins | Follow-up Study
-
NCT07616115CompletedVenous Insufficiency | Varicose Veins of Lower Limb | Saphenous Vein
-
NCT01909024UnknownVaricose Veins | Venous Reflux | Pelvic Congestion Syndrome
-
NCT04526626UnknownVaricose Veins of Lower Limb
-
NCT03653793Completed