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Comparison Between Intralesional Injection of Plasma Rich Platelets and Candida Antigen in Plane Warts

S

South Valley University

Status and phase

Active, not recruiting
Phase 4

Conditions

Plane Wart

Treatments

Biological: C. albicans antigen
Other: saline
Other: autologous PRP

Study type

Interventional

Funder types

Other

Identifiers

NCT05652998
233/9/21

Details and patient eligibility

About

To compare the efficacy of intralesional injection of autologous plasma rich platelets and candida antigen in treatment of patients with plane warts .

Full description

Cutaneous warts are benign tumors caused by infection of keratinocytes by different serotypes of human papillomavirus(HPV). Its incidence increases during the school years to reach a peak in adolescence and early adulthood, then declines rapidly through the twenties and more gradually thereafter.

Plane warts are mainly caused by HPV serotypes 3, 10, 28, and 41, presenting mainly in children and young adults. They present as skin colored or may be hyperpigmented smooth-surfaced, slightly elevated or flat-topped papules. They are polygonal or round in shape and range in sizes from 1 to 5 mm. The main sites of predilection for the plane warts are the face, dorsal aspects of the hands and forearms, often in a linear array.

Platelet rich plasma (PRP) is an autologous blood-derived product enriched in platelets. Platelets, also called thrombocytes, are blood cells that cause blood clots and other necessary growth healing functions. PRP represents a new bio technology that is part of the growing interest in tissue engineering and cellular therapy today. While it is of autologous origin, it reduces the possibility of adverse effects and transfusion-transmitted infections, so it is well-tolerated therapy for the patients. PRP has been used in the treatment of many cutaneous diseases such as alopecia and acne vulgaris. Its utility has been extended to other cutaneous diseases as melasma, hyperpigmentation, and burns, wherever it elicits tissue repair and regeneration.

Intralesional immunotherapy depends on the ability of the immune system to recognize certain viral, bacterial, and fungal antigens, such as Candida or Trichophyton antigens that induce a delayed-type hypersensitivity reaction, not only to the antigen but also against the wart virus, which in turn increases the ability of the immune system to recognize and eradicate HPV. This stimulated immune response could then subsequently destroy all the injected and noninjected lesions on the body, rather than the locally treated lesion.

Intralesional antigen immunotherapy has recently received increased attention and is considered by many authors a promising modality for the treatment of different types of warts, including the recurrent and recalcitrant variants.

Enrollment

30 estimated patients

Sex

All

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patients proved as having clinically evident plane warts.
  • Patients with both sexes with no age limits.

Exclusion criteria

  • Patient receiving immune suppressive drugs.
  • Patients with major comorbidities or concomitant malignancies.
  • Patients with any evidence of immunosuppression including HIV infection.
  • Patients with any eczematous skin disorder
  • Those with any history of hypersensitivity to Candida albicans antigen.
  • Patients with chronic systemic medical diseases and bleeding disorders .

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

30 participants in 3 patient groups, including a placebo group

Candida antigen
Active Comparator group
Description:
patients will be injected with intralesional C.albicans antigen
Treatment:
Biological: C. albicans antigen
Autologous platelets rich plasma
Active Comparator group
Description:
patients will receive intralesional autologous PRP injection
Treatment:
Other: autologous PRP
Saline
Placebo Comparator group
Description:
patients will receive intralesional saline
Treatment:
Other: saline

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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