Skip to content

Efficacy of Maggot therapy on burning ulcers

A clinical study on efficacy of maggot therapy for treatment of 3rd grade of burning ulcers

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20170531034272N2
Enrollment
24
Registered
2018-07-24
Start date
2018-08-23
Completion date
Unknown
Last updated
2018-09-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Burning ulcers of grade 3. Burn and corrosion of trunk, shoulder and upper limb, wrist and hand, hip and lower limb, ankle and foot

Interventions

Intervention 1: Intervention group: Maggot therapy (use of larvae of Lucilia sericata) will use beside of routine therapeutic measures. Routine therapy may be involves local and systemic measures, va

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who have at least one burning ulcer (3rd grade) with bacterial infection. Patients who have not need anticoagulant or steroid pharmaceutics. Patients who have not acute or other chronic diseases. Patients who have ?not addicted to alcohol or opium. Patients who have not Osteomyelitis. Patients who have not entomophobia.

Exclusion criteria

Exclusion criteria: Patients who have sever diseases such as heart disorders and so on during maggot Therapy. Patients who get sever and un-controlled fever during maggot therapy. Patients who have sever pain during maggot Therapy. Patients with maceration around the wound after each interval of maggot therapy. Patients who take bleeding during maggot therapy.

Design outcomes

Primary

MeasureTime frame
Measuring the necrotic tissues. Timepoint: 48 and 96 hours after starting of treatment. Method of measurement: Photographing and measuring by MATLAB 1.6, the mathwork inc, natic, ma, 2000.

Secondary

MeasureTime frame
Bacterial infections, Staphilococcus aureus and Pseudomonas aeruginosa. Timepoint: 48 and 96 hours after treatment. Method of measurement: culturing of samples in laboratory.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactJavad Rafinejad

Tehran University of Medical Sciences

jrafinejad@tums.ac.ir+98 21 4293 3121

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026