Maggot Debridement Therapy Versus Conventional Dressing Therapy to Treat Diabetic Foot Ulcers

Diabetic Foot Ulcers Clinical Trial

— MDTDF  

Official title:

Maggot Debridement Therapy Versus Conventional Dressing Therapy to Treat Type 2 Diabetic Mellitus Foot Ulcers: A Prospective Randomized Controlled Study

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT02816749
• Other study ID #: DMUF-01
• Status: Recruiting
• Phase: Phase 4
• First received: April 26, 2016
• Last updated: June 30, 2016
• Start date: June 2016
• Est. completion date: February 2017

Study information

• Verified date: June 2016
• Source: The First Affiliated Hospital of Dalian Medical University
• Contact: Jun-Wei Zong
• Phone: 8618098876071
• Email: aweizone[@]163.com
• Is FDA regulated: No
• Health authority: China: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

This is a prospective study of participants with diabetic foot ulcers who will receive either maggot debridement therapy (MDT) or conventional dressing therapy (CDT). Wound healing time is the main outcome measure to compare the clinical efficacy of these two therapies. The investigators developed a hypothesis that MDT could achieve remarkable shorter time and better healing rate for wound closure when compared with CDT.

Description:

The investigators designed a prospective randomized study to compare the clinical safety and efficacy of maggot debridement therapy (MDT) and conventional dressing therapy (CDT). This study is scheduled from July 2016 to February 2017. Patients, aged from 18-80, who suffered from type 2 diabetic mellitus foot ulcers with Grade 1 or Grade 2 according to the Wagner classification could be the participants of this study. A sample of 138 participants was calculated based on the morbidity of diabetic foot ulcers, accounting for estimated 10% attrition rate. The glycemic control is important for the validity of study results. A specific team of endocrine doctors will manage the blood glucose of participants of two groups within the range of 7-10 mmol/L.

Participants will be allocated into MDT group and CDT group randomly according to the random number table. For MDT-participants, bio-bags containing sterilized, live, medicinal Lucilia sericata larvae will be placed on the wound of ulcers. For CDT-participants, conventional dressing (disinfected by iodophor, dressed by gauze ) will be performed ordinally. Every 3 days the procedures of two groups will be performed and wounds assessment will be done until the wounds closure is achieved. The wounds assessment, including measurement of the area of wound surface and bacterial culture, will be performed by a specific team of microsurgical doctors. The outcome measures include wound healing time (days) and the time negative bacterial culture occurs (days). The secondary outcome measures include the area of wound surface (cm2), treatment related pain, comfort of the dressing and adverse events.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 138
• Est. completion date: February 2017
• Est. primary completion date: December 2016
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 80 Years

Eligibility

Inclusion Criteria:

1. Participants aged from 18-80 years old.

2. Participants with type 2 diabetes mellitus longer than one year, foot ulcer longer than three weeks and with ischemic symptoms of lower limb.

3. The ulcer erosion depth is not reached and muscle layer.

4. The Wagner classification of ulcers should be Grade 1 or Grade 2.

5. Blood glucose control: Fasting blood glucose = 8mmol / L; Postprandial blood glucose two hours = 11.1 mmol / L.

6. Participants do not receive ulcer wound management in the past three days when recruited.

7. Participants with neuropathy symptoms, such as limb numbness, tingling or pain, especially pain at night.

Exclusion Criteria:

1. Participants with acute thrombosis that required thrombolysis or thrombectomy.

2. Participants with severe systemic infection.

3. Participants who are sensitive to pain.

4. Participants with bone/joint deformities of foot (eagle claw toes, hammer toes)

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Diabetic Foot
• Diabetic Foot Ulcers
• Foot Ulcer
• Ulcer

Intervention

Procedure:
• Maggot debridement therapy
Participant will receive bio-bags treatment every 3 days until the wound heal completely, when wounds assessed.
• Conventional Dressing Therapy
Participant will be disinfected by iodophor and dressed by gauze 3 days until the wound heal completely, when wounds assessed.

Locations

Country	Name	City	State
China	the First Affiliated Hospital of Dalian Medical University	Dalian	Liaoning
China	the Second Affiliated Hospital of Dalian Medical University	Dalian	Liaoning

Sponsors (1)

Lead Sponsor	Collaborator
The First Affiliated Hospital of Dalian Medical University

Country where clinical trial is conducted

China, 

References & Publications (4)

Pinheiro MA, Ferraz JB, Junior MA, Moura AD, da Costa ME, Costa FJ, Neto VF, Neto RM, Gama RA. Use of maggot therapy for treating a diabetic foot ulcer colonized by multidrug resistant bacteria in Brazil. Indian J Med Res. 2015 Mar;141(3):340-2. — View Citation

Sherman RA, Shapiro CE, Yang RM. Maggot therapy for problematic wounds: uncommon and off-label applications. Adv Skin Wound Care. 2007 Nov;20(11):602-10. — View Citation

Shi E, Shofler D. Maggot debridement therapy: a systematic review. Br J Community Nurs. 2014 Dec;Suppl Wound Care:S6-13. doi: 10.12968/bjcn.2014.19.Sup12.S6. Review. — View Citation

Sun X, Jiang K, Chen J, Wu L, Lu H, Wang A, Wang J. A systematic review of maggot debridement therapy for chronically infected wounds and ulcers. Int J Infect Dis. 2014 Aug;25:32-7. doi: 10.1016/j.ijid.2014.03.1397. Epub 2014 May 16. Review. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Wound healing time(days)	Wound complete closure is achieved.	From date of randomization until the date of the complete closure of wound or up to 12 weeks, whichever came first.	No
Secondary	Area of wounds (cm2)	Area of wounds are measured by transparency-based digital imaging method.Every 3/4 days when procedures(bio-bags/dressings) given.	From date of randomization until the date of the complete closure of wound or up to 12 weeks, whichever came first.	No
Secondary	Adverse events	Adverse events such as allergic reaction, infection, local pain and escape of the larvae from bio-bag.Every 3/4 day when procedures(bio-bags/dressings) given.	From date of randomization until the date of the complete closure of wound or up to 12 weeks, whichever came first.	No
Secondary	Negative bacterial culture time (days)	The time that negative bacterial culture occured from recruitment.	From date of randomization until the date of the complete closure of wound or up to 12 weeks, whichever came first.	No