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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01681160
Other study ID # 86/116
Secondary ID
Status Completed
Phase N/A
First received September 4, 2012
Last updated September 7, 2012
Start date January 2009
Est. completion date June 2011

Study information

Verified date September 2012
Source Kerman Medical University
Contact n/a
Is FDA regulated No
Health authority Iran: Ministry of Health
Study type Interventional

Clinical Trial Summary

This study was a Kind of clinical trial with equal randomization, that have been done from January 2009 to June 2011 in the AFZALIPOOR hospital endocrine ward in Kerman-Iran on 128 diabetic patient who had foot wounds.Replacement of conventional therapy by new methodes is one of the more important aims for health professional specially for nurses.One of this new treatment is maggot therapy.


Recruitment information / eligibility

Status Completed
Enrollment 128
Est. completion date June 2011
Est. primary completion date December 2009
Accepts healthy volunteers No
Gender Both
Age group 40 Years to 90 Years
Eligibility Inclusion Criteria:

- Have a chronic illness more than 7 weeks.

- The age of the patients between 40- 90 years old.

- Not having capillary disease (Blockage of artery, Rinold).

- Not user of anticoagulants and corticosteroids drugs.

- Patients without history of allergy to drugs and foods.

- Having diabetic type 2

Exclusion Criteria:

- patients who refer to critical clinical care unit

- patients who have amputation

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Other:
procedure:maggot therapy
each times in maggot therapy continued for three days.wound assessment was done before and after any intervention
conventional therapy
patients receive ordinary treatment for diabetic foot

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Kerman Medical University

Outcome

Type Measure Description Time frame Safety issue
Primary change from baseline in BATES-JENSEN WOUND ASSESSMENT score at 3days and change from baseline in BATES-JENSEN WOUND ASSESSMENT score at 6 days 2 years No
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