Skip to content

Production of Cord Blood Platelet Gel (CBPG) for treatment of burn ulcer

Comparing the effect of adding cord blood platelet gel (CBPG) to the standard treatment on granulation tissue formation and time of wound healing in second degree burn ulcer

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20141007019432N4
Enrollment
15
Registered
2018-01-16
Start date
2018-03-11
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

burn and ulcer. Burn of second degree of wrist and hand

Interventions

Intervention 1: Intervention group: Including persons who have burn of ulcers on their hands larger than 10 and less than 20 cm2, aged between to 20 until 40 years old and their burn ulcer is clas
Intervention group: Including persons who have burn of ulcers on their hands larger than 10 and less than 20 cm2, aged between to 20 until 40 years old and their burn ulcer is classified as second
Control group: At the same time, the same group of patients who have another wound on their hands receive dressing including routine treatment (without the use of a platelet gel derived from umbilical

Sponsors

Vice Presidency for Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: Patients that have second degree burn of ulcer Age between 20 to 40 years The burn of ulcer should be on the hand. The burn of ulcer should be second degree and deep. Both of genders can be entered this study. The surface of ulcer should be more than 10 cm2 and less than 20 cm2

Exclusion criteria

Exclusion criteria: The patients that they have some diseases such as diabetes, allergy and coagulopathy If the burns of ulcers are first or third degree The burn of ulcer that has a very low or high surface area

Design outcomes

Primary

MeasureTime frame
Area of granulation tissue formation. Timepoint: before intervention and 6 days after last intervention. Method of measurement: pictzar software.;Area and depth of the wound. Timepoint: before intervention and 6 days after last intervention. Method of measurement: pictzar software.

Secondary

MeasureTime frame
Pain from the burn of ulcer. Timepoint: 6 days after the first intervention. Method of measurement: Question and answer from the patient.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Amir Amirkhani

Tehran University of Medical Sciences

elham_torkamaniha@yahoo.com+98 21 2220 1710

Outcome results

None listed

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