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Clinical Trials/NCT06450015
NCT06450015CompletedNot Applicable

Comparison of Vacuum Assisted Closure and Saline Dressing in Patients With Diabetic Foot Ulcers

Children Hospital and Institute of Child Health, Lahore2 sites in 1 country88 target enrollmentStarted: January 1, 2022Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
88
Locations
2
Primary Endpoint
time to wound healing

Study Overview

Brief Summary

Conventionally diabetic foot is treated with moist wound dressing and antibiotics but recent studies show that VAC dressing gives better results as compared to conventional saline dressing in treating Diabetic Foot Ulcers. This may decrease amputations rate, work load on hospitals, hospital stay, repeated hospital admissions, unemployment and can improve patient's quality of life. Objective of the study was to compare the effectiveness of Vacuum Assisted Closure therapy with saline dressing in management of diabetic foot ulcers in terms of granulation tissue formation and wound healing.

Detailed Description

it was a randomized Controlled Trial done in department of Surgery, Mayo Hospital,vLahore, Pakistan from January 2022 to July 2022. Patients divided in two groups, in the VAC group (Group A), the wound bed was filled with a saline soaked gauze piece after it is thoroughly cleaned. VAC was applied by placing sterile pads in two layers with a 16Fr Ryle's tube placed between the two layers and then the wound was sealed by a sterile transparent polyurethane sheet. The tube was connected to a wall mounted suction device and the pressure was set at -125 mmHg. In the Saline group (Group B), normal saline dressing was given. This consists of placing a saline soaked gauze piece over the wound bed after cleaning the wound. Patients were assessed and followed for wound healing. The primary outcome parameter was time taken to complete wound healing. Secondary outcome parameters were granulation tissue formation using a visual score and complication of bleeding, pain, and infection. Only healthy granulation tissue which appears pink was considered for scoring assessment. Infection was assessed by wound culture sensitivity which was sent every week.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 60 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • • Diabetic foot ulcer (DFU) patients between the ages of 18 and 60
  • Patients of both genders
  • Diabetic foot ulcer (DFU) patients whose ulcers are smaller than 15 cm in diameter.

Exclusion Criteria

  • • Coagulopathy
  • Venous diseases
  • Foot Ulcers with underlying Osteomyelitis
  • Charcot's joint
  • Peripheral Vascular Diseases
  • Patients with Wegener's Grade IV
  • Involving both feet
  • Patients with HIV and Chronic Liver Disease

Outcomes

Primary Outcomes

time to wound healing

Time Frame: 1 month

total time for wound healing was assessed.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Children Hospital and Institute of Child Health, Lahore
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Muhammad Adeel Ashiq

Principal Investigator

Children Hospital and Institute of Child Health, Lahore

Study Sites (2)

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