The biological dressing and conventional treatment in patients with massive burn: a clinical trial

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

ISRCTN

Registry ID

ISRCTN01055688

Enrollment

118

Registered

2006-09-25

Start date

2002-10-01

Completion date

Unknown

Last updated

2015-01-13

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

Conditions

Burns Injury, Occupational Diseases, Poisoning Burns

Interventions

The patients were divided into two groups: 1. Those in the first group (conventional treatment) did not have satisfying wounds for treatment with biological dressings. This group were treated by daily

Eligibility

Inclusion criteria

Inclusion criteria: The patients had Total Body Surface Area (TBSA) between 30% to 75% due to scalds or flames.

Exclusion criteria

Exclusion criteria: Non-infected and non-chemical burns.

Design outcomes

Primary

Measure	Time frame
1. Mechanism of injury 2. TBSA 3. Total hospital stay 4. Amount of serum until started per oral feeding use 5. Number of oral or injectable analgesic intake 6. The number of dressing association with inhalation injury 7. Mortality	—

Secondary

Measure	Time frame
Albumin and Fresh Frozen Plasma (FFP) intake.	—

Countries

Iran

Outcome results

None listed

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