Clinical trial

Efficacy of Intralesional Voriconazole Versus Intralesional Cryotherapy Versus Intralesional Sodium Stibogluconate Versus Oral Doxycycline in the Treatment of Acute Cutaneous Leishmaniasis

Name
ZU-IRB#8095/3-10-2021
Description
Leishmaniasis is a vector-borne disease caused by obligate, intracellular protozoa of the genus Leishmania and transmitted by phlebotomine sandflies. It is found mostly in tropical and subtropical areas then it has spread into southern Europe. Increased international travel and immigration have led to an increased diagnosis of leishmaniasis cases in nonendemic areas (Kollipara et al., 2016). Foci of CL, caused by L. ma¬jor, occur in Afghanistan, Egypt, Iran, Iraq, Jordan, Libya, Morocco, Palestine, Pakistan, Saudi Arabia, Sudan, Syria, Tunisia, and Yemen. Many researchers have studied leishmaniasis in the endemic northern African countries, e.g., Morocco, Algeria, Tunisia, Egypt, and Libya. One of the established endemic leishmaniasis Libyan provinces is Al-jabal Al-gharbi province, where CL comprises a major parasitic health problem (Abdellatif et al., 2013).To evaluate the efficacy of intralesional cryotherapy, intralesional Voriconazole, and oral doxycycline in the treatment of cutaneous leishmaniasis compared to the conventional treatment (intralesional SSG).
Trial arms
Trial start
2022-01-01
Estimated PCD
2023-12-01
Trial end
2024-03-01
Status
Recruiting
Phase
Early phase I
Treatment
Intralesional Sodium stibogluconate
Sessions will be held once weekly for a maximum of 6 weeks
Arms:
Intralesional Sodium stibogluconate
Other names:
SSG
Intralesional Cryotherapy
Intralesional Cryotherapy. Sessions will be held every two weeks
Arms:
intralesional Cryotherapy
Intralesional Voriconazole
Weekly intralesional Voriconazole
Arms:
Intralesional Voriconazole
Other names:
Vfend
Oral doxycycline
200 mg daily for 6 weeks or till complete cure
Arms:
Oral doxycycline
Size
136
Primary endpoint
Clinical response to treatment
6 weeks
Eligibility criteria
Inclusion Criteria: * All participants must be willing to sign informed consent, for patients younger than 18 years old, parents or guardians will sign an informed consent. 1. Patients clinically diagnosed with cutaneous leishmaniasis and confirmed using parasitological Giemsa-stained direct smears. 2. Acute lesions of less than 12-week duration to exclude any possibility of natural self-healing of the lesions during follow-up. 3. Both sexes. 4. Age: \> 12 years old. Exclusion Criteria: * • Pregnancy and lactation. * Patients \< 12 years old. * Patients with negative Giemsa stained direct smears. * Patients with concomitant renal or liver impairment, congestive heart failure, uncontrolled diabetes mellitus, peripheral neuropathy, poor peripheral circulation, and prolonged corticosteroid therapy. * Patients with lesions of more than 12 weeks duration. * Patients with lesions \> 5cm2 * History of anti-Leishmania therapy in the last 3 months. * For the intralesional groups the presence of \> 5 lesions. * Lesions in the perimeter (\< 2 cm) of mucosal areas e.g. eyes, nose, mouth, or genitals. * Patients with known hypersensitivity or allergy to the assigned drugs.
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE3'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'PARALLEL', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'DOUBLE', 'whoMasked': ['PARTICIPANT', 'INVESTIGATOR']}}, 'enrollmentInfo': {'count': 136, 'type': 'ESTIMATED'}}
Updated at
2023-08-29

1 organization

3 products

2 indications

Organization
Zagazig University
Indication
Leishmaniasis
Indication
Cutaneous