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Comparison of Platelet-Rich Plasma Dressing and Normal Saline Dressing for Wound Healing in Patients With Chronic Diabetic Wounds

Comparison of Platelet-Rich Plasma Dressing and Normal Saline Dressing for Wound Healing in Patients With Chronic Diabetic Wounds

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06867328
Enrollment
156
Registered
2025-03-10
Start date
2024-11-10
Completion date
2025-05-10
Last updated
2025-05-31

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

Conditions

Diabetic Ulcers, Diabetic Wounds

Keywords

Platelet-Rich Plasma (PRP), Normal Saline Dressing, Diabetic Ulcers, Chronic Wounds

Brief summary

Chronic diabetic wounds are a major health concern, often taking a long time to heal and increasing the risk of complications like infections and amputations. This study aims to compare the effectiveness of Platelet-Rich Plasma (PRP) Dressing versus Normal Saline Dressing in the treatment of chronic diabetic wounds. PRP is a treatment derived from the patient's own blood that contains growth factors, which may accelerate wound healing. Participants with chronic diabetic wounds will be randomly assigned to receive either PRP dressing or normal saline dressing. The study will measure the rate of wound healing and the time taken to achieve complete healing in both groups. It is hypothesized that PRP dressing will lead to faster and more effective wound healing compared to normal saline dressing. Findings from this research could help improve wound care strategies for diabetic patients and provide evidence for a more effective treatment approach in clinical practice.

Detailed description

After obtaining approval from the institutional review board and obtaining informed consent from study participants, all patients fulfilling the inclusion criteria were included in the study from the surgery indoor department of Gulab Devi Hospital, Lahore. Baseline characteristics, including age (in years), gender (male/female), and history of comorbidities (hypertension/ischemic heart disease/smoking), were assessed by reviewing previous medical records and taking a detailed history. The duration of diabetes (in years), duration of the wound (weeks), size of the wound (measured using a millimeter scale along the longest axis), and class of chronic diabetic wound (III/IV) were documented. After wound debridement, patients were randomized into two equal groups by block randomization as follows: Group A: Patients were managed with normal saline dressing. Group B: Patients were managed with PRP dressing. In this technique, the wound was washed with normal saline, and platelet-rich plasma (prepared from the patient's own blood by the hematology department) was injected into the surrounding wound area twice weekly, followed by the placement of a gauze over it. Dressing was continued for a period of 6 weeks or until wound healing was achieved, whichever was shorter. To assess healing, all patients in both groups were followed up weekly until 6 weeks (study endpoint). The duration required to achieve wound healing was also documented. Additionally, 6 weeks post-therapy, wound size was reassessed. In cases of non-healing, alternative therapy was provided based on the wound condition and the consultant surgeon's advice. All data were recorded in a predesigned proforma and kept confidential.

Interventions

PROCEDUREPlatelet-Rich Plasma (PRP) Dressing

* PRP will be prepared by centrifugation of 20 mL venous blood with an anticoagulant. * The extracted PRP will be applied twice weekly to the wound. * A sterile gauze will be placed over the wound after PRP application. * Treatment will continue for up to 6 weeks or until wound healing is achieved.

Wound will be cleansed with normal saline and covered with sterile gauze. * Dressing changes will be done twice weekly following wound debridement. * Treatment will continue for up to 6 weeks or until wound healing is achieved.

Sponsors

Gulab Devi Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Age 18-60 years. * Either male or female. * Chronic diabetic wound. * Wagner class III and IV.

Exclusion criteria

* Wound sustained \< 6 weeks from time of presentation. * Previous history of PRP dressing use, assessed by reviewing previous medical records. * History of hypersensitivity to PRP, assessed by reviewing previous medical records. * Burn injury, assessed by reviewing previous medical records. * Class I, II and V.

Design outcomes

Primary

MeasureTime frameDescription
Wound HealingEvaluated weekly for up to 6 weeksWound healing will be assessed based on the formation of pinkish granulation tissue completely covering the wound. The healing status will be determined by a consultant surgeon through visual inspection.

Secondary

MeasureTime frameDescription
Duration to Achieve Wound HealingMeasured at the end of 6 weeks or at the point of complete wound healing, whichever occurs first.The duration required for complete wound healing (formation of granulation tissue covering the entire wound) will be recorded in weeks for each patient in both groups.

Countries

Pakistan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026