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Effectiveness, Safety and Feasibility of HECT-CL, in Quetta, Pakistan (HECT-CL)

Primary Purpose

Cutaneous Leishmaniases

Status
Terminated
Phase
Phase 3
Locations
Pakistan
Study Type
Interventional
Intervention
HECT-CL
Sponsored by
Medecins Sans Frontieres, Netherlands
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cutaneous Leishmaniases focused on measuring thermotherapy, Pakistan

Eligibility Criteria

10 Years - undefined (Child, Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion criteria

  • Patients with clinical CL symptoms for less than 6 months with the diagnosis confirmed by microscopic visualisation of Leishmania parasites in skin scrape smear.
  • Patients who have given written informed consent.

Exclusion criteria

  • Patients presenting with CL lesions located on or within two centimetres of eyes and lips.
  • Patients with more than four lesions.
  • Lesions, nodules and/or ulcerations with a diameter (ø) of more than 6 cm.
  • Patients with persistent lesions for more than 6 months.
  • Patients younger than 10 years.
  • Patients who are unlikely, unable or unwilling to be available for and comply to regular follow up visits for 6 months.
  • Pregnant, and lactating women <6 months after delivery.
  • Patients with uncontrolled medical illnesses.
  • Patients with immune disorders, such as HIV/AIDS, or those who are on steroid medication

Sites / Locations

  • Mohtarma Shaheed Benazir Bhutto Hospital Quetta.

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

HECT-CL

Arm Description

HECT-CL heat pack will be applied on CL lesions (50-52 degrees Celsius for 3 minutes on 7 consecutive days)

Outcomes

Primary Outcome Measures

Effectiveness of the HECT-CL treatment as assessed by
The proportion of patients with complete re-epithelisation at each follow up visit associated with the HECT-CL treatment
Possible adverse effect of the HECT-CL treatment will studied by
The proportion of patients experiencing adverse effects (AEs) and serious adverse effects (SAEs) (Safety)
Ease of use of the HECT-CL treatment as assessed by
the observation of, and feedback from health providers on the ease of (re-)use of the HECT-CL (feasibility).
Acceptability of the HECT-CL treatment as assessed by
proportion of patients completing the treatment schedule in time (feasibility)
Inappropriateness of the HECT-CL treatment as assessed by
the percentage of patients (%) with lesions where HECT-CL cannot be used, (e.g. near eyes and lips, larger than 6 cm, or more than four lesions) (feasibility)

Secondary Outcome Measures

The scars remaining after the HECT-CL treatment as assessed by
the proportion of patients with remaining scars
The duration of the healing process as assessed by
The mean time (days) between time of start of treatment and complete re-epithelisation of the treated lesion the healing of the lesion (time-to-heal).

Full Information

First Posted
May 26, 2017
Last Updated
January 14, 2019
Sponsor
Medecins Sans Frontieres, Netherlands
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1. Study Identification

Unique Protocol Identification Number
NCT03208543
Brief Title
Effectiveness, Safety and Feasibility of HECT-CL, in Quetta, Pakistan
Acronym
HECT-CL
Official Title
Effectiveness, Safety and Feasibility of Thermotherapy With the Hand-held Exothermic Crystallization Thermotherapy for Cutaneous Leishmaniasis (HECT-CL), Device for Cutaneous Leishmaniasis in Quetta, Pakistan
Study Type
Interventional

2. Study Status

Record Verification Date
January 2019
Overall Recruitment Status
Terminated
Why Stopped
failure rate 91.1%
Study Start Date
October 4, 2017 (Actual)
Primary Completion Date
December 20, 2017 (Actual)
Study Completion Date
December 20, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Medecins Sans Frontieres, Netherlands

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This research studies the effect thermotherapy as treatment of Old World CL which is not invasive, non-toxic, and the short treatment. While the current standard treatment comprise daily painful injections with antimonials,
Detailed Description
The current standard treatment for Old World CL is based on daily painful injections with antimonials, which in Pakistan requires specialised care provided in secondary level care facilities. Apart from potential toxic side effects of these antimonials, the long treatment course, high cost and inconvenience, it may prevent patients from seeking care or completing treatment, especially women and children in the Pakistan context. Untreated cutaneous leishmaniasis may leave disfiguring scars leading to stigmatisation and (psycho) social problems. If the CL lesions/scars are located on joints they can cause problems in motion and lead to disability. At a public health level, patients with untreated CL lesions are a reservoir for further transmission of CL in the family and community. Thermotherapy is topical, not invasive, non-toxic, and the treatment duration is only 7 days, and therefore is expected to have major benefits for patients. Additional advantages are that the HECT-CL can be applied by lower level qualified health workers, and the costs are low (less than 3 USD) per re-usable heat pad), and therefore can be rolled out to peripheral health facilities, potentially having a major impact on access to treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cutaneous Leishmaniases
Keywords
thermotherapy, Pakistan

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Single Group Assignment
Model Description
Patients meeting inclusion criteria will be enrolled to receive seven treatment sessions with thermotherapy (HECT-CL device) and will be reassessed during follow up visits at day 15, 30, 60, 90 and 180
Masking
None (Open Label)
Allocation
N/A
Enrollment
56 (Actual)

8. Arms, Groups, and Interventions

Arm Title
HECT-CL
Arm Type
Experimental
Arm Description
HECT-CL heat pack will be applied on CL lesions (50-52 degrees Celsius for 3 minutes on 7 consecutive days)
Intervention Type
Device
Intervention Name(s)
HECT-CL
Intervention Description
To evaluate the effectiveness, safety and feasibility of thermotherapy with the low cost Hand-held Exothermic Crystallization Thermotherapy pad in the treatment of cutaneous leishmaniasis in Quetta, Balochistan, Pakistan.
Primary Outcome Measure Information:
Title
Effectiveness of the HECT-CL treatment as assessed by
Description
The proportion of patients with complete re-epithelisation at each follow up visit associated with the HECT-CL treatment
Time Frame
180 days
Title
Possible adverse effect of the HECT-CL treatment will studied by
Description
The proportion of patients experiencing adverse effects (AEs) and serious adverse effects (SAEs) (Safety)
Time Frame
180 days
Title
Ease of use of the HECT-CL treatment as assessed by
Description
the observation of, and feedback from health providers on the ease of (re-)use of the HECT-CL (feasibility).
Time Frame
180 days
Title
Acceptability of the HECT-CL treatment as assessed by
Description
proportion of patients completing the treatment schedule in time (feasibility)
Time Frame
180 days
Title
Inappropriateness of the HECT-CL treatment as assessed by
Description
the percentage of patients (%) with lesions where HECT-CL cannot be used, (e.g. near eyes and lips, larger than 6 cm, or more than four lesions) (feasibility)
Time Frame
180 days
Secondary Outcome Measure Information:
Title
The scars remaining after the HECT-CL treatment as assessed by
Description
the proportion of patients with remaining scars
Time Frame
180 days
Title
The duration of the healing process as assessed by
Description
The mean time (days) between time of start of treatment and complete re-epithelisation of the treated lesion the healing of the lesion (time-to-heal).
Time Frame
180 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
10 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion criteria Patients with clinical CL symptoms for less than 6 months with the diagnosis confirmed by microscopic visualisation of Leishmania parasites in skin scrape smear. Patients who have given written informed consent. Exclusion criteria Patients presenting with CL lesions located on or within two centimetres of eyes and lips. Patients with more than four lesions. Lesions, nodules and/or ulcerations with a diameter (ø) of more than 6 cm. Patients with persistent lesions for more than 6 months. Patients younger than 10 years. Patients who are unlikely, unable or unwilling to be available for and comply to regular follow up visits for 6 months. Pregnant, and lactating women <6 months after delivery. Patients with uncontrolled medical illnesses. Patients with immune disorders, such as HIV/AIDS, or those who are on steroid medication
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Koert Ritmeijer, PhD
Organizational Affiliation
Medecins Sans Frontieres, Netherlands
Official's Role
Study Director
Facility Information:
Facility Name
Mohtarma Shaheed Benazir Bhutto Hospital Quetta.
City
Quetta
State/Province
Baluchistan
ZIP/Postal Code
00000
Country
Pakistan

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
25842586
Citation
Shah SA, Memon AA, Auwj-e-Shamim, Baqi S, Witzig R. Low-cost thermotherapy for cutaneous leishmaniasis in Sindh, Pakistan. J Pak Med Assoc. 2014 Dec;64(12):1398-404.
Results Reference
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PubMed Identifier
23556016
Citation
Olliaro P, Vaillant M, Arana B, Grogl M, Modabber F, Magill A, Lapujade O, Buffet P, Alvar J. Methodology of clinical trials aimed at assessing interventions for cutaneous leishmaniasis. PLoS Negl Trop Dis. 2013;7(3):e2130. doi: 10.1371/journal.pntd.0002130. Epub 2013 Mar 21.
Results Reference
background
PubMed Identifier
15791515
Citation
Reithinger R, Mohsen M, Wahid M, Bismullah M, Quinnell RJ, Davies CR, Kolaczinski J, David JR. Efficacy of thermotherapy to treat cutaneous leishmaniasis caused by Leishmania tropica in Kabul, Afghanistan: a randomized, controlled trial. Clin Infect Dis. 2005 Apr 15;40(8):1148-55. doi: 10.1086/428736. Epub 2005 Mar 16.
Results Reference
background
PubMed Identifier
23658851
Citation
Valencia BM, Miller D, Witzig RS, Boggild AK, Llanos-Cuentas A. Novel low-cost thermotherapy for cutaneous leishmaniasis in Peru. PLoS Negl Trop Dis. 2013 May 2;7(5):e2196. doi: 10.1371/journal.pntd.0002196. Print 2013.
Results Reference
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Effectiveness, Safety and Feasibility of HECT-CL, in Quetta, Pakistan

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