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Adrenaline Reduces Ecchymoses and Hematomas and Improves Quality of Life After Classic Saphenous Vein Stripping (ARESQOLSAVES)

Primary Purpose

Venous Insufficiency (Chronic)(Peripheral), Venous Reflux, Venous Insufficiency of Leg

Status
Completed
Phase
Not Applicable
Locations
Greece
Study Type
Interventional
Intervention
Great saphenous vein stripping and varicectomies
Epinephrine Topical
normal saline
Sponsored by
Junior Doctors Network-Hellas
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Venous Insufficiency (Chronic)(Peripheral) focused on measuring great saphenous vein, saphenectomy, saphenous vein stripping, ecchymosis, haematoma, adrenaline, epinephrin, hemostasis, chronic venous insufficiency, venous reflux, venous disease

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age 18-80 years
  • CVI CEAP Class II or III
  • Informed consent signed

Exclusion Criteria:

  • Age <18 or >80 years
  • CVI CEAP Class I or IV (venous ulcers)
  • Allergy to adrenaline history
  • No informed consent signed

Sites / Locations

  • Department of Vascular Surgery, Andreas Papandreou General Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Sham Comparator

Sham Comparator

Arm Label

Group A

Group B

Group C

Arm Description

Group A - great saphenous vein stripping with local adrenaline use for hemostasis

Group B - great saphenous vein stripping with local normal saline use for hemostasis

Group C - great saphenous vein stripping with traditional hemostatic practice

Outcomes

Primary Outcome Measures

Subcutaneous ecchymoses number 1d-postop
The absolute number of subcutaneous ecchymoses on the operated limb on 1st post-operative day
Subcutaneous ecchymoses number 8d-post-op
The absolute number of subcutaneous ecchymoses on the operated limb on 8th post-operative day
Subcutaneous ecchymoses number 14d-post-op
The absolute number of subcutaneous ecchymoses on the operated limb on 14th post-operative day
Subcutaneous hematomas number 1d-postop
The absolute number of subcutaneous hematomas in the operated limb on 1st post-operative day
Subcutaneous hematomas number 8d-postop
The absolute number of subcutaneous hematomas in the operated limb on 8th post-operative day
Subcutaneous hematomas number 14d-postop
The absolute number of subcutaneous hematomas in the operated limb on 14th post-operative day
Subcutaneous ecchymoses total area 1d-postop
The total area in mm2 of subcutaneous ecchymoses in the operated limb on 1st post-operative day
Subcutaneous ecchymoses total area 8d-postop
The total area in mm2 of subcutaneous ecchymoses in the operated limb on 8th post-operative day
Subcutaneous ecchymoses total area 14d-postop
The total area in mm2 of subcutaneous ecchymoses in the operated limb on 14th post-operative day
Subcutaneous hematomas total area 1d-postop
The total area in mm2 of subcutaneous hematomas in the operated limb on 1st post-operative day
Subcutaneous hematomas total area 8d-postop
The total area in mm2 of subcutaneous hematomas in the operated limb on 8th post-operative day
Subcutaneous hematomas total area 14d-postop
The total area in mm2 of subcutaneous hematomas in the operated limb on 14th post-operative day
QoL-SF36 preop
Quality of life assessment based on the 36-Item Short Form Survey (SF-36) questionnaire preoperatively. It is an often-used, well-researched, self-reported measure of health. It stems from a study called the Medical Outcomes Study. It taps eight health concepts: physical functioning, bodily pain, role limitations due to physical health problems, role limitations due to personal or emotional problems, emotional well-being, social functioning, energy/fatigue, and general health perceptions. It also includes a single item that provides an indication of perceived change in health. The eight scaled scores, which are the weighted sums of the questions in their section are directly transformed into a 0-100 scale on the assumption that each question carries equal weight. The lower the score the more disability. The higher the score the less disability i.e., a score of zero is equivalent to maximum disability and a score of 100 is equivalent to no disability.
QoL-SF36 1month-postop
Quality of life assessment based on the 36-Item Short Form Survey (SF-36) questionnaire 30 days post-operatively. It is an often-used, well-researched, self-reported measure of health. It stems from a study called the Medical Outcomes Study. It taps eight health concepts: physical functioning, bodily pain, role limitations due to physical health problems, role limitations due to personal or emotional problems, emotional well-being, social functioning, energy/fatigue, and general health perceptions. It also includes a single item that provides an indication of perceived change in health. The eight scaled scores, which are the weighted sums of the questions in their section are directly transformed into a 0-100 scale on the assumption that each question carries equal weight. The lower the score the more disability. The higher the score the less disability i.e., a score of zero is equivalent to maximum disability and a score of 100 is equivalent to no disability.
QoL-CIVIQ2 preop
Quality of life assessment based on the ChronIc Venous Insufficiency quality of life Questionnaire version 2 (CIVIQ-2) questionnaire preoperatively. The CIVIQ was developed and validated (relevance, acceptability, reliability, construct validity, and sensitivity) by French researchers in 1996. The CIVIQ is a 20-item self-reported instrument that includes four categories of questions: physical (4 items), psychological (9 items), social (4 items), and pain (3 items). Its score ranges from 0, the worst score, to 100, the best. There are five possible answers (from 1 to 5) to describe each symptom and the sensation of discomfort. The second version, the CIVIQ-2 (where 2 denotes the second draft of the same questionnaire), provides a global score covering all aspects of the questionnaire and weighs the categories equally.
QoL-CIVIQ2 1month post-op
Quality of life assessment based on the CIVIQ-2 questionnaire 1 month post-operatively. Quality of life assessment based on the ChronIc Venous Insufficiency quality of life Questionnaire version 2 (CIVIQ-2) questionnaire preoperatively. The CIVIQ was developed and validated (relevance, acceptability, reliability, construct validity, and sensitivity) by French researchers in 1996. The CIVIQ is a 20-item self-reported instrument that includes four categories of questions: physical (4 items), psychological (9 items), social (4 items), and pain (3 items). Its score ranges from 0, the worst score, to 100, the best. There are five possible answers (from 1 to 5) to describe each symptom and the sensation of discomfort. The second version, the CIVIQ-2 (where 2 denotes the second draft of the same questionnaire), provides a global score covering all aspects of the questionnaire and weighs the categories equally.

Secondary Outcome Measures

HCT preop
Hematocrit (HCT) measured pre-operatively, in percentage (%).
HCT postop
Hematocrit (HCT) measured post-operatively, in percentage (%).
Hgb preop
Hemoglobin (Hgb) measured pre-operatively, in mg/dL.
Hgb postop
Hemoglobin (Hgb) measured post-operatively, in mg/dL.
WBC preop
White blood cells (WBC) count measured pre-operatively, in K/mcL.
WBC postop
White blood cells (WBC) count measured post-operatively, in K/mcL.
PLT preop
Platelet count (PLT) measured pre-operatively, in K/mcL.
PLT postop
Platelet count (PLT) measured post-operatively, in K/mcL.
FIB preop
Fibrinogen (FIB) measured pre-operatively, in mg/dL.
FIB postop
Fibrinogen (FIB) measured post-operatively, in mg/dL.
ESR preop
Erythrocyte sedimentation rate on the 1st hour, measured pre-operatively, in millimeters (mm).
ESR postop
Erythrocyte sedimentation rate on the 1st hour, measured post-operatively, in millimeters (mm).
CRP preop
Serum C-reactive protein (CRP) measured pre-operatively, in mg/L.
CRP postop
Serum C-reactive protein (CRP) measured post-operatively, in mg/L.
Experienced pain preop
Pain experienced pre-operatively assessed by a numeric rating pain scale (0-10). Numeric Rating Scale (NRS-11) is an 11-point scale for patient self-reporting of pain. It is for adults and children 10 years old or older. 0 indicates no pain, 5 moderate and 10 worst possible pain.
Experienced pain 1d-postop
Pain experienced pre-operatively assessed by a numeric rating pain scale (0-10). Numeric Rating Scale (NRS-11) is an 11-point scale for patient self-reporting of pain. It is for adults and children 10 years old or older. 0 indicates no pain, 5 moderate and 10 worst possible pain.
Experienced pain 8d-postop
Pain experienced pre-operatively assessed by a numeric rating pain scale (0-10). Numeric Rating Scale (NRS-11) is an 11-point scale for patient self-reporting of pain. It is for adults and children 10 years old or older. 0 indicates no pain, 5 moderate and 10 worst possible pain.
Experienced pain 14d-postop
Pain experienced pre-operatively assessed by a numeric rating pain scale (0-10). Numeric Rating Scale (NRS-11) is an 11-point scale for patient self-reporting of pain. It is for adults and children 10 years old or older. 0 indicates no pain, 5 moderate and 10 worst possible pain.

Full Information

First Posted
February 9, 2021
Last Updated
February 17, 2021
Sponsor
Junior Doctors Network-Hellas
Collaborators
General Hospital of Rhodes Andreas Papandreou, Hellenic Red Cross Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT04758728
Brief Title
Adrenaline Reduces Ecchymoses and Hematomas and Improves Quality of Life After Classic Saphenous Vein Stripping
Acronym
ARESQOLSAVES
Official Title
The Role of Adrenaline in the Reduction of Subcutaneous Ecchymoses and Hematomas and in the Improvement of the Quality of Life of Patients After Classic Great Saphenous Vein Stripping
Study Type
Interventional

2. Study Status

Record Verification Date
February 2021
Overall Recruitment Status
Completed
Study Start Date
September 10, 2015 (Actual)
Primary Completion Date
May 14, 2016 (Actual)
Study Completion Date
June 10, 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Junior Doctors Network-Hellas
Collaborators
General Hospital of Rhodes Andreas Papandreou, Hellenic Red Cross Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Aim of the present study is to investigate the efficiency of adrenaline (epinephrine) used locally in reducing and avoiding post-operative formation of subcutaneous ecchymoses and hematomas, in comparison with traditional practice of hemostasis, and to assess improvement in the quality of life of subjects undergoing classic great saphenous vein stripping, who received or did not receive adrenaline as a local hemostatic.
Detailed Description
Introduction Quality of life of subjects undergoing classic great saphenous vein stripping is analogous of the gravity of subcutaneous ecchymoses and hematomas formation, as a result of surgical interventions during open surgery, when the great saphenous vein is being removed. Adrenaline (epinephrine) is a potent vasoconstrictor, whose local hemostatic ability has already been documented and applied in many medical specialties. Aim of the present study to investigate the efficiency of adrenaline (epinephrine) used locally in reducing and avoiding post-operative formation of subcutaneous ecchymoses and hematomas, in comparison with traditional practice of hemostasis, and to assess improvement in the quality of life of subjects undergoing classic great saphenous vein stripping, who received or did not receive adrenaline as a local hemostatic. Material-Methods 40 subjects diagnosed with chronic venous insufficiency (CVI) and/or varicose veins of the lower limbs of varied clinical gravity (CEAP classification II & III), admitted in the department of Vascular Surgery for open surgical management, i.e. great saphenous vein stripping +/- removal of varicosities, will be enrolled after signing an informed consent for their participation in the study. They will be then randomized into 3 separate groups: Group A - great saphenous vein stripping with local adrenaline use for hemostasis Group B - great saphenous vein stripping with local normal saline use for hemostasis Group C - great saphenous vein stripping with traditional hemostatic practice Study subjects will be followed-up after surgery, and in each group measurement of ecchymoses (small 2-5mm2 and large >5mm2) and hematomas (medium 0,2-1cm and large >1cm) will be performed by using ImageJ software after digital high-resolution photographing on 1st, 8th and 14th post-operative days. Quality of life of subjects will be assessed pre-operatively and 1 month post-operatively, by using SF-36 and CIVIQ-2 questionnaires for QoL in CVI.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Venous Insufficiency (Chronic)(Peripheral), Venous Reflux, Venous Insufficiency of Leg, Venous Stasis, Venous Disease, Subcutaneous Haematoma, Ecchymosis, Bruising
Keywords
great saphenous vein, saphenectomy, saphenous vein stripping, ecchymosis, haematoma, adrenaline, epinephrin, hemostasis, chronic venous insufficiency, venous reflux, venous disease

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
40 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Group A
Arm Type
Active Comparator
Arm Description
Group A - great saphenous vein stripping with local adrenaline use for hemostasis
Arm Title
Group B
Arm Type
Sham Comparator
Arm Description
Group B - great saphenous vein stripping with local normal saline use for hemostasis
Arm Title
Group C
Arm Type
Sham Comparator
Arm Description
Group C - great saphenous vein stripping with traditional hemostatic practice
Intervention Type
Procedure
Intervention Name(s)
Great saphenous vein stripping and varicectomies
Other Intervention Name(s)
Saphenectomy
Intervention Description
Removal of the great saphenous vein (partially - from just below the knee up to the saphenofemoral junction) by two 3cm skin and subcutaneous fat incisions and the introduction of a conventional vein stripper device, under general or epidural/regional anesthesia. Removal of varicose veins of the lower limb by 0,5cm skin incisions and the use of a conventional phlebectomy stainless steel hook. Mechanical hemostasis by direct compression of the thigh for 10 minutes.
Intervention Type
Drug
Intervention Name(s)
Epinephrine Topical
Other Intervention Name(s)
Adrenaline solution 1:1000 topical/local use
Intervention Description
Use of epinephrine/adrenaline solution 1:1000 topically
Intervention Type
Drug
Intervention Name(s)
normal saline
Other Intervention Name(s)
NaCl 0,9% topical/local use
Intervention Description
Use of normal saline solution NaCl 0,9% topically
Primary Outcome Measure Information:
Title
Subcutaneous ecchymoses number 1d-postop
Description
The absolute number of subcutaneous ecchymoses on the operated limb on 1st post-operative day
Time Frame
24 hours post-operatively
Title
Subcutaneous ecchymoses number 8d-post-op
Description
The absolute number of subcutaneous ecchymoses on the operated limb on 8th post-operative day
Time Frame
192 hours post-operatively
Title
Subcutaneous ecchymoses number 14d-post-op
Description
The absolute number of subcutaneous ecchymoses on the operated limb on 14th post-operative day
Time Frame
336 hours post-operatively
Title
Subcutaneous hematomas number 1d-postop
Description
The absolute number of subcutaneous hematomas in the operated limb on 1st post-operative day
Time Frame
24 hours post-operatively
Title
Subcutaneous hematomas number 8d-postop
Description
The absolute number of subcutaneous hematomas in the operated limb on 8th post-operative day
Time Frame
192 hours post-operatively
Title
Subcutaneous hematomas number 14d-postop
Description
The absolute number of subcutaneous hematomas in the operated limb on 14th post-operative day
Time Frame
336 hours post-operatively
Title
Subcutaneous ecchymoses total area 1d-postop
Description
The total area in mm2 of subcutaneous ecchymoses in the operated limb on 1st post-operative day
Time Frame
24 hours post-operatively
Title
Subcutaneous ecchymoses total area 8d-postop
Description
The total area in mm2 of subcutaneous ecchymoses in the operated limb on 8th post-operative day
Time Frame
192 hours post-operatively
Title
Subcutaneous ecchymoses total area 14d-postop
Description
The total area in mm2 of subcutaneous ecchymoses in the operated limb on 14th post-operative day
Time Frame
336 hours post-operatively
Title
Subcutaneous hematomas total area 1d-postop
Description
The total area in mm2 of subcutaneous hematomas in the operated limb on 1st post-operative day
Time Frame
24 hours post-operatively
Title
Subcutaneous hematomas total area 8d-postop
Description
The total area in mm2 of subcutaneous hematomas in the operated limb on 8th post-operative day
Time Frame
192 hours post-operatively
Title
Subcutaneous hematomas total area 14d-postop
Description
The total area in mm2 of subcutaneous hematomas in the operated limb on 14th post-operative day
Time Frame
336 hours post-operatively
Title
QoL-SF36 preop
Description
Quality of life assessment based on the 36-Item Short Form Survey (SF-36) questionnaire preoperatively. It is an often-used, well-researched, self-reported measure of health. It stems from a study called the Medical Outcomes Study. It taps eight health concepts: physical functioning, bodily pain, role limitations due to physical health problems, role limitations due to personal or emotional problems, emotional well-being, social functioning, energy/fatigue, and general health perceptions. It also includes a single item that provides an indication of perceived change in health. The eight scaled scores, which are the weighted sums of the questions in their section are directly transformed into a 0-100 scale on the assumption that each question carries equal weight. The lower the score the more disability. The higher the score the less disability i.e., a score of zero is equivalent to maximum disability and a score of 100 is equivalent to no disability.
Time Frame
24 hours pre-operatively
Title
QoL-SF36 1month-postop
Description
Quality of life assessment based on the 36-Item Short Form Survey (SF-36) questionnaire 30 days post-operatively. It is an often-used, well-researched, self-reported measure of health. It stems from a study called the Medical Outcomes Study. It taps eight health concepts: physical functioning, bodily pain, role limitations due to physical health problems, role limitations due to personal or emotional problems, emotional well-being, social functioning, energy/fatigue, and general health perceptions. It also includes a single item that provides an indication of perceived change in health. The eight scaled scores, which are the weighted sums of the questions in their section are directly transformed into a 0-100 scale on the assumption that each question carries equal weight. The lower the score the more disability. The higher the score the less disability i.e., a score of zero is equivalent to maximum disability and a score of 100 is equivalent to no disability.
Time Frame
30 days post-operatively
Title
QoL-CIVIQ2 preop
Description
Quality of life assessment based on the ChronIc Venous Insufficiency quality of life Questionnaire version 2 (CIVIQ-2) questionnaire preoperatively. The CIVIQ was developed and validated (relevance, acceptability, reliability, construct validity, and sensitivity) by French researchers in 1996. The CIVIQ is a 20-item self-reported instrument that includes four categories of questions: physical (4 items), psychological (9 items), social (4 items), and pain (3 items). Its score ranges from 0, the worst score, to 100, the best. There are five possible answers (from 1 to 5) to describe each symptom and the sensation of discomfort. The second version, the CIVIQ-2 (where 2 denotes the second draft of the same questionnaire), provides a global score covering all aspects of the questionnaire and weighs the categories equally.
Time Frame
24 hours pre-operatively
Title
QoL-CIVIQ2 1month post-op
Description
Quality of life assessment based on the CIVIQ-2 questionnaire 1 month post-operatively. Quality of life assessment based on the ChronIc Venous Insufficiency quality of life Questionnaire version 2 (CIVIQ-2) questionnaire preoperatively. The CIVIQ was developed and validated (relevance, acceptability, reliability, construct validity, and sensitivity) by French researchers in 1996. The CIVIQ is a 20-item self-reported instrument that includes four categories of questions: physical (4 items), psychological (9 items), social (4 items), and pain (3 items). Its score ranges from 0, the worst score, to 100, the best. There are five possible answers (from 1 to 5) to describe each symptom and the sensation of discomfort. The second version, the CIVIQ-2 (where 2 denotes the second draft of the same questionnaire), provides a global score covering all aspects of the questionnaire and weighs the categories equally.
Time Frame
30 days post-operatively
Secondary Outcome Measure Information:
Title
HCT preop
Description
Hematocrit (HCT) measured pre-operatively, in percentage (%).
Time Frame
24 hours pre-operatively
Title
HCT postop
Description
Hematocrit (HCT) measured post-operatively, in percentage (%).
Time Frame
24 hours post-operatively
Title
Hgb preop
Description
Hemoglobin (Hgb) measured pre-operatively, in mg/dL.
Time Frame
24 hours pre-operatively
Title
Hgb postop
Description
Hemoglobin (Hgb) measured post-operatively, in mg/dL.
Time Frame
24 hours post-operatively
Title
WBC preop
Description
White blood cells (WBC) count measured pre-operatively, in K/mcL.
Time Frame
24 hours pre-operatively
Title
WBC postop
Description
White blood cells (WBC) count measured post-operatively, in K/mcL.
Time Frame
24 hours post-operatively
Title
PLT preop
Description
Platelet count (PLT) measured pre-operatively, in K/mcL.
Time Frame
24 hours pre-operatively
Title
PLT postop
Description
Platelet count (PLT) measured post-operatively, in K/mcL.
Time Frame
24 hours post-operatively
Title
FIB preop
Description
Fibrinogen (FIB) measured pre-operatively, in mg/dL.
Time Frame
24 hours pre-operatively
Title
FIB postop
Description
Fibrinogen (FIB) measured post-operatively, in mg/dL.
Time Frame
24 hours post-operatively
Title
ESR preop
Description
Erythrocyte sedimentation rate on the 1st hour, measured pre-operatively, in millimeters (mm).
Time Frame
24 hours pre-operatively
Title
ESR postop
Description
Erythrocyte sedimentation rate on the 1st hour, measured post-operatively, in millimeters (mm).
Time Frame
24 hours post-operatively
Title
CRP preop
Description
Serum C-reactive protein (CRP) measured pre-operatively, in mg/L.
Time Frame
24 hours pre-operatively
Title
CRP postop
Description
Serum C-reactive protein (CRP) measured post-operatively, in mg/L.
Time Frame
24 hours post-operatively
Title
Experienced pain preop
Description
Pain experienced pre-operatively assessed by a numeric rating pain scale (0-10). Numeric Rating Scale (NRS-11) is an 11-point scale for patient self-reporting of pain. It is for adults and children 10 years old or older. 0 indicates no pain, 5 moderate and 10 worst possible pain.
Time Frame
24 hours pre-operatively
Title
Experienced pain 1d-postop
Description
Pain experienced pre-operatively assessed by a numeric rating pain scale (0-10). Numeric Rating Scale (NRS-11) is an 11-point scale for patient self-reporting of pain. It is for adults and children 10 years old or older. 0 indicates no pain, 5 moderate and 10 worst possible pain.
Time Frame
24 hours post-operatively
Title
Experienced pain 8d-postop
Description
Pain experienced pre-operatively assessed by a numeric rating pain scale (0-10). Numeric Rating Scale (NRS-11) is an 11-point scale for patient self-reporting of pain. It is for adults and children 10 years old or older. 0 indicates no pain, 5 moderate and 10 worst possible pain.
Time Frame
192 hours post-operatively
Title
Experienced pain 14d-postop
Description
Pain experienced pre-operatively assessed by a numeric rating pain scale (0-10). Numeric Rating Scale (NRS-11) is an 11-point scale for patient self-reporting of pain. It is for adults and children 10 years old or older. 0 indicates no pain, 5 moderate and 10 worst possible pain.
Time Frame
336 hours post-operatively

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 18-80 years CVI CEAP Class II or III Informed consent signed Exclusion Criteria: Age <18 or >80 years CVI CEAP Class I or IV (venous ulcers) Allergy to adrenaline history No informed consent signed
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Konstantinos Roditis, MD, MSc
Organizational Affiliation
JDN-Hellas / Department of Vascular Surgery, Hellenic Red Cross Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Dimitrios Mavros, MD, MSc, PhD
Organizational Affiliation
Department of Vascular Surgery, Andreas Papandreou General Hospital
Official's Role
Study Chair
Facility Information:
Facility Name
Department of Vascular Surgery, Andreas Papandreou General Hospital
City
Rhodes
State/Province
South Aegean
ZIP/Postal Code
85133
Country
Greece

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
1522653
Citation
Furuya T, Tada Y, Sato O. A new technique for reducing subcutaneous hemorrhage after stripping of the great saphenous vein. J Vasc Surg. 1992 Sep;16(3):493-4. doi: 10.1016/0741-5214(92)90389-p. No abstract available.
Results Reference
background
PubMed Identifier
16236532
Citation
Nisar A, Shabbir J, Tubassam MA, Shah AR, Khawaja N, Kavanagh EG, Grace PA, Burke PE. Local anaesthetic flush reduces postoperative pain and haematoma formation after great saphenous vein stripping--a randomised controlled trial. Eur J Vasc Endovasc Surg. 2006 Mar;31(3):325-31. doi: 10.1016/j.ejvs.2005.08.006. Epub 2005 Oct 19.
Results Reference
background
PubMed Identifier
16047519
Citation
Pappa E, Kontodimopoulos N, Niakas D. Validating and norming of the Greek SF-36 Health Survey. Qual Life Res. 2005 Jun;14(5):1433-8. doi: 10.1007/s11136-004-6014-y.
Results Reference
background
PubMed Identifier
16158038
Citation
Andreozzi GM, Cordova RM, Scomparin A, Martini R, D'Eri A, Andreozzi F; Quality of Life Working Group on Vascular Medicine of SIAPAV. Quality of life in chronic venous insufficiency. An Italian pilot study of the Triveneto Region. Int Angiol. 2005 Sep;24(3):272-7.
Results Reference
background
PubMed Identifier
32028367
Citation
Kim H, Hwang K, Yun SM, Kim DJ. Usage of Epinephrine Mixed With Lidocaine in Plastic Surgery. J Craniofac Surg. 2020 May/Jun;31(3):791-793. doi: 10.1097/SCS.0000000000006156.
Results Reference
background

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Adrenaline Reduces Ecchymoses and Hematomas and Improves Quality of Life After Classic Saphenous Vein Stripping

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