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Photodynamic Therapy in Treatment of Verrucae

A

Alexandria University

Status

Unknown

Conditions

Verruca Vulgaris

Treatments

Other: saline
Other: methylene blue / IPL
Other: IPL

Study type

Interventional

Funder types

Other

Identifiers

NCT04620785
0106171

Details and patient eligibility

About

To assess the efficacy (clinically and dermoscopically) and safety of photodynamic therapy using intralesional injection of 4% methylene blue solution as a photosensitizer with IPL versus IPL only in treatment of warts.

Full description

This study will be conducted on:

Eighty patients suffering of verruca (male and female) divided randomly into three groups: group A, B&C :

Group A: 30 patients will undergo photodynamic therapy using intralesional 4%methylene blue solution and IPL.

Group B: 30 patients will undergo IPL only. Group C (control group):20 patients will undergo intralesional saline.

Enrollment

80 estimated patients

Sex

All

Ages

16+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Age:Above 16 years old.
  2. Sex:Both males and female patients.
  3. Clinically and dermoscopically documented verruca.
  4. No verruca treatment in the last 2 weeks.

Exclusion criteria

  1. History of photosensitivity disorder.
  2. Pregnant and lactating females.
  3. Diseases with risk of koebnerization e.g. Psoriasis and Lichen planus.
  4. Anogenital warts.
  5. Warts on head and neck.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

80 participants in 3 patient groups, including a placebo group

methylene blue/IPL
Experimental group
Description:
will undergo photodynamic therapy using intralesional 4%methylene blue solution ,after a period of 15 minutes the patient will be subjected to IPL session. This will be repeated biweekly until complete clearance of the lesion or a maximum four sessions.
Treatment:
Other: methylene blue / IPL
IPL
Experimental group
Description:
will undergo biweekly IPL sessions only until complete clearance of the lesion or a maximum four sessions.
Treatment:
Other: IPL
saline
Placebo Comparator group
Description:
will undergo intralesional saline.
Treatment:
Other: saline

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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