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Polidocanol Versus Glucose Treatment of Telangiectasia Trial (PG3T)

Primary Purpose

Varicose Veins, Telangiectasis

Status
Completed
Phase
Phase 4
Locations
Brazil
Study Type
Interventional
Intervention
Glucose
Polidocanol with Glucose
Sponsored by
UPECLIN HC FM Botucatu Unesp
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Varicose Veins focused on measuring telangiectasis, varicose veins, veins, glucose, sclerotherapy

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • females
  • with telangiectasis on thigh side
  • clinical classification of chronic venous disease C1(mild venous disease),
  • minimum age of 18 year-old and maximum age 65 year-old
  • agreement with the study
  • signing the free and informed consent ( IC)
  • not use anticoagulant drugs .

Exclusion Criteria:

  • male
  • varicose disease in any quantity or location with clinical classification of chronic venous disease different of C1(mild venous disease)
  • restrict mobility
  • arterial insufficiency
  • be allergic to any substance that may be related to the study drugs
  • any cause of dermatitis on application site
  • don´t be free of comorbidities clinically serious as diabetes mellitus, heart failure, respiratory failure, uncontrolled hypertension with medication, and uncontrolled hypothyroidism
  • pregnancy
  • previous deep vein thrombosis (DVT)
  • family history of DVT
  • thrombophilia
  • do not agree with the search terms

Sites / Locations

  • Vascular Lab

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Glucose

Polidocanol with Glucose

Arm Description

An application session 0.2% Polidocanol + 70% Glucose to treat telangiectasis of the lower limb selected, with a maximum volume of 5 ml. Return to a week to investigate the adverse effects and 2 months for proof of efficacy and adverse effects

An application session 0.2% Polidocanol + 70% Glucose to treat telangiectasis of the lower limb selected, with a maximum volume of 5 ml. Return to a week to investigate the adverse effects and 2 months for proof of efficacy and adverse effects

Outcomes

Primary Outcome Measures

Change From Baseline in Extent of Telangiectasias
Efficiency in promoting the disappearance of the treated telangiectasias, making the comparison between the initial measurements in centimeters and after two months, then comparing the treatment between the two treatments

Secondary Outcome Measures

Skin Hyperpigmentation
Observed after two months of treatment the occurrence of hyperpigmentation stains in the treated areas. Measuring in centimeters those stains and compare the two treatments together.
Number of Participants With Deep Venous Thrombosis (DVT)
Observe after one week of treatment occurred if clinical signs and symptoms of deep vein thrombosis (DVT) and perform duplex ultrasound for confirmation. Compare the results between the two groups to establish a security policy.

Full Information

First Posted
January 7, 2016
Last Updated
November 30, 2017
Sponsor
UPECLIN HC FM Botucatu Unesp
Collaborators
Fundação de Amparo à Pesquisa do Estado de São Paulo
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1. Study Identification

Unique Protocol Identification Number
NCT02657252
Brief Title
Polidocanol Versus Glucose Treatment of Telangiectasia Trial
Acronym
PG3T
Official Title
Polidocanol Versus Glucose For Sclerotherapy Treatment Of Telangiectasia Of The Lower Limbs: Protocol For A Randomized, Controlled Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
November 2017
Overall Recruitment Status
Completed
Study Start Date
January 2015 (undefined)
Primary Completion Date
September 2016 (Actual)
Study Completion Date
November 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
UPECLIN HC FM Botucatu Unesp
Collaborators
Fundação de Amparo à Pesquisa do Estado de São Paulo

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
It will be done a randomized triple-blind study comparing 0,2% polidocanol versus 75% hypertonic glucose of sclerotherapy in lower limbs´ telangiectasis. It will be included only adult women with reticular veins on the side of the thighs and mild venous insufficiency (CEAP 1). The primary endpoint will be efficacy, and secondary will be safety.
Detailed Description
Background. The prevalence of chronic venous disease is high in the general population, mainly in young women, and in milder cases the usual complaint is aesthetic. Various techniques are used for treatment of mild varicose disease, including surgical treatment, laser ablation and sclerotherapy. Telangiectasis are those with less than 1 mm diameter, reddish and important contribution to the aesthetic damage, and sometimes they are related to local pain. There is no consensus in the literature about the effectiveness of treatment with sclerotherapy, despite of being an usual procedure with different chemicals. Methods and design. One hundred lower limbs of healthy women between 18 and 65 years will be triple blind randomized to receive treatment with polidocanol 0.2% diluted in 70% hypertonic glucose versus 75% hypertonic glucose for sclerotherapy treatment of telangiectasis. The patients will be examined and clinically classified. It will be included patients with telangiectasis sited at out's thigh, and only one extremity will be included per patient. The patients with varicose disease CEAP 2 or more will not be included. The treatment will be carried out in only one session and the medication volume not exceeding 5 ml. Clinical follow-up protocols will be filled on regular visits on days 0 - 7 - 60 concomitantly with photograph documentation. Supplementary examination for venous mapping with ultrasound pretreatment is performed for all patients. Discussion. This prospective controlled double-blind randomized trial aims to verify and compare the efficacy and safety for sclerotherapy treatment of telangiectasis of the lower limbs. The results may help physicians to choose the best sclerotherapy treatment for telangiectasis.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Varicose Veins, Telangiectasis
Keywords
telangiectasis, varicose veins, veins, glucose, sclerotherapy

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
115 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Glucose
Arm Type
Active Comparator
Arm Description
An application session 0.2% Polidocanol + 70% Glucose to treat telangiectasis of the lower limb selected, with a maximum volume of 5 ml. Return to a week to investigate the adverse effects and 2 months for proof of efficacy and adverse effects
Arm Title
Polidocanol with Glucose
Arm Type
Active Comparator
Arm Description
An application session 0.2% Polidocanol + 70% Glucose to treat telangiectasis of the lower limb selected, with a maximum volume of 5 ml. Return to a week to investigate the adverse effects and 2 months for proof of efficacy and adverse effects
Intervention Type
Drug
Intervention Name(s)
Glucose
Other Intervention Name(s)
Hypertonic dextrose
Intervention Description
Sclerotherapy of telangiectasis in one lower limb.
Intervention Type
Drug
Intervention Name(s)
Polidocanol with Glucose
Other Intervention Name(s)
Asclera, Varithena
Intervention Description
Sclerotherapy of telangiectasis in one lower limb.
Primary Outcome Measure Information:
Title
Change From Baseline in Extent of Telangiectasias
Description
Efficiency in promoting the disappearance of the treated telangiectasias, making the comparison between the initial measurements in centimeters and after two months, then comparing the treatment between the two treatments
Time Frame
2 months
Secondary Outcome Measure Information:
Title
Skin Hyperpigmentation
Description
Observed after two months of treatment the occurrence of hyperpigmentation stains in the treated areas. Measuring in centimeters those stains and compare the two treatments together.
Time Frame
2 months
Title
Number of Participants With Deep Venous Thrombosis (DVT)
Description
Observe after one week of treatment occurred if clinical signs and symptoms of deep vein thrombosis (DVT) and perform duplex ultrasound for confirmation. Compare the results between the two groups to establish a security policy.
Time Frame
1 week

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: females with telangiectasis on thigh side clinical classification of chronic venous disease C1(mild venous disease), minimum age of 18 year-old and maximum age 65 year-old agreement with the study signing the free and informed consent ( IC) not use anticoagulant drugs . Exclusion Criteria: male varicose disease in any quantity or location with clinical classification of chronic venous disease different of C1(mild venous disease) restrict mobility arterial insufficiency be allergic to any substance that may be related to the study drugs any cause of dermatitis on application site don´t be free of comorbidities clinically serious as diabetes mellitus, heart failure, respiratory failure, uncontrolled hypertension with medication, and uncontrolled hypothyroidism pregnancy previous deep vein thrombosis (DVT) family history of DVT thrombophilia do not agree with the search terms
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Matheus Bertanha, Dr
Organizational Affiliation
Botucatu School of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Vascular Lab
City
Botucatu
State/Province
São Paulo
ZIP/Postal Code
18618687
Country
Brazil

12. IPD Sharing Statement

Plan to Share IPD
Yes
Citations:
PubMed Identifier
27684809
Citation
Bertanha M, Camargo PA, Moura R, Yoshida WB, Pimenta RE, Mariuba JV, Alcantara GP, de Paula DR, Sobreira ML. Polidocanol versus glucose in the treatment of telangiectasia of the lower limbs (PG3T): Protocol for a randomized, controlled clinical trial. Medicine (Baltimore). 2016 Sep;95(39):e4812. doi: 10.1097/MD.0000000000004812.
Results Reference
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Polidocanol Versus Glucose Treatment of Telangiectasia Trial

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