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Efficacy of Radio-frequency Induced Heat (RFH)Therapy in Treatment of Cutaneous Leishmaniasis in India

Primary Purpose

Cutaneous Leishmaniasis

Status
Completed
Phase
Phase 4
Locations
India
Study Type
Interventional
Intervention
RFH therapy
Sodium stibogluconate
Sponsored by
Sarder Patel Medical College
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cutaneous Leishmaniasis focused on measuring cutaneous leishmaniasis, heat therapy, antimony

Eligibility Criteria

1 Year - 90 Years (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • parasitologically confirmed diagnosis of cutaneous leishmaniasis

Exclusion Criteria:

  • Multiple lesions (more than 4)

Sites / Locations

  • PBM Hospita and SP Medical College

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Sodium stibogluconate

RFH therapy

Arm Description

Intralesional SSG was administered in dose of 50 mg cm -2 of lesion once a week for 6 weeks (total six injections)

RFH therapy was administered by a single, controlled and localized delivery of radio frequencies into the lesion for 30-60 seconds under local anesthesia (1% lidocaine) using a current field radio-frequency generator (ThermoMed 1.8, Thermosurgery Inc).

Outcomes

Primary Outcome Measures

Time to heal lesion

Secondary Outcome Measures

Tissue scarring
Recurrence/Relapse of lesion

Full Information

First Posted
August 7, 2012
Last Updated
August 31, 2012
Sponsor
Sarder Patel Medical College
Collaborators
Ohio State University
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1. Study Identification

Unique Protocol Identification Number
NCT01661296
Brief Title
Efficacy of Radio-frequency Induced Heat (RFH)Therapy in Treatment of Cutaneous Leishmaniasis in India
Official Title
An Open Label Study of RFH Therapy as Treatment for CL Caused by Leishmania Tropica in India
Study Type
Interventional

2. Study Status

Record Verification Date
August 2012
Overall Recruitment Status
Completed
Study Start Date
August 2009 (undefined)
Primary Completion Date
August 2011 (Actual)
Study Completion Date
December 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Sarder Patel Medical College
Collaborators
Ohio State University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Infections caused by the protozoan parasite Leishmania include cutaneous (CL), mucosal (ML) and visceral leishmaniasis (VL). Over 12 million people currently suffer from leishmaniasis, and approximately 2 million new cases occur annually, making it a major global health problem. CL CL caused by Leishmania tropica is endemic around the city of Bikaner in Thar Desert region of the State of Rajasthan . WHO recommends antimonials such as sodium stibogluconate (SSG) to treat CL. However, these drugs are toxic and have poor patient compliance as they require multiple intramuscular or intralesional injections for 3 weeks. In addition, the emergence of drug-resistant strains is rapidly increasing worldwide. We are interested in novel treatments for CL that are safe, easy to administer and effective in inducing long-term cure. Recently, radio-frequency-induced heat (RFH) therapy has been used to treat CL. This treatment involves the controlled and localized delivery of radiofrequencies into lesions for 30-60 seconds under local anesthesia. Several short-term follow-up (4-5 months) studies as well as one long-term follow-up (12 months) study involving US soldiers who were infected with L. major in Iraq found that RFH therapy was comparable, or even better, than systemic antimonials. However, more studies are needed to establish long-term efficacy of RFH therapy in treatment of CL caused by other Leishmania species that are difficult to treat with conventional drugs, and to determine the risk of disease recurrence if any in patients living in Leishmania endemic regions. The goal of this trial is to compare long term efficacy of RFH therapy in treatment of CL caused by L. tropica in patients residing in Leishmania-endemic regions of India.
Detailed Description
Study location and participants: Subjects for this study were recruited among children between the ages of 1-17 and adults between the ages of 18-85 who visit the dermatology outpatient clinic at PBM Hospital, Bikaner, with suspected CL. Informed consent was obtained from adults or from parents/legal guardians of minors for procedures and inclusion in the study. Individuals with any uncontrolled chronic medical condition, breast feeding, on immunosuppressive drugs or anticipated unavailability for follow-up were excluded from the study. Patients with more than 4 lesions were also excluded. Study procedures: The diagnosis of CL was established by clinical examination, history of residence in an L. tropica-endemic area, and by microscopic examination of Giemsa-stained lesion smears for parasites (Leishmania tropica bodies) or lesion biopsy. For patients who were both smear and skin biopsy negative, PCR was used to detect parasites in the lesion tissue. The lesion and surrounding skin were cleaned with stabilized 0.1% chlorine dioxide solution, and local anesthesia was administered by subcutaneous injection of 2% Lidocaine around the lesion. RFH therapy was administered by a single, controlled and localized delivery of radio frequencies into the lesion for 30-60 seconds using a current field radio-frequency generator (ThermoMed 1.8; Thermosurgery Inc. USA). Patients were be prescribed an oral NSAID and topical antimicrobial cream for 5 days. Cure of infection and any recurrence was monitored by clinical follow-up at days 10 and months 1, 2, 3, 4, 6, 9, 12 and 18 months post-treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cutaneous Leishmaniasis
Keywords
cutaneous leishmaniasis, heat therapy, antimony

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
100 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Sodium stibogluconate
Arm Type
Active Comparator
Arm Description
Intralesional SSG was administered in dose of 50 mg cm -2 of lesion once a week for 6 weeks (total six injections)
Arm Title
RFH therapy
Arm Type
Active Comparator
Arm Description
RFH therapy was administered by a single, controlled and localized delivery of radio frequencies into the lesion for 30-60 seconds under local anesthesia (1% lidocaine) using a current field radio-frequency generator (ThermoMed 1.8, Thermosurgery Inc).
Intervention Type
Other
Intervention Name(s)
RFH therapy
Other Intervention Name(s)
Heat therapy
Intervention Description
RFH therapy was administered by a single, controlled and localized delivery of radio frequencies into the lesion for 30-60 seconds under local anesthesia using a current field radio-frequency generator.
Intervention Type
Drug
Intervention Name(s)
Sodium stibogluconate
Other Intervention Name(s)
Glucantine, SSG
Intervention Description
Six intralesional injections (one injection per week) of SSG 50mg/cm-2 area of lesions
Primary Outcome Measure Information:
Title
Time to heal lesion
Time Frame
6 months after treatment
Secondary Outcome Measure Information:
Title
Tissue scarring
Time Frame
12 months
Title
Recurrence/Relapse of lesion
Time Frame
18 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Year
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: parasitologically confirmed diagnosis of cutaneous leishmaniasis Exclusion Criteria: Multiple lesions (more than 4)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ram A Bumb, MD
Organizational Affiliation
PBM Hospital and SP Medical College, Bikaner, Rajasthan, India
Official's Role
Principal Investigator
Facility Information:
Facility Name
PBM Hospita and SP Medical College
City
Bikaner
State/Province
Rajasthan
Country
India

12. IPD Sharing Statement

Learn more about this trial

Efficacy of Radio-frequency Induced Heat (RFH)Therapy in Treatment of Cutaneous Leishmaniasis in India

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