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Evaluation of therapeutic effect of Quercus infectoria gall on pressure ulcer in patients with cerebral palsy

Evaluation of therapeutic effect of Quercus infectoria gall on pressure ulcer in patients with cerebral palsy due stroke

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017080435420N2
Enrollment
94
Registered
2017-08-17
Start date
2017-08-06
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

Pressure ulcer. Decubitus ulcer and pressure area, unspecified

Interventions

Intervention 1: Intervention: local application of Phenytoin cream 1% once daily in areas susceptible to ulcer (sacrum
iliac
spinal cord
waist
shoulder
auricle
buttock
heel and ankle) to the extent that cover the wound area and local application of Q. infectoria gall extract in the cream tube that is similar to placebo at 12 hours later for two weeks. Intervention 2
heel and ankle) to the extent that cover the wound area and local application of placebo in the cream tube that is similar to drug at 12 hours later for two weeks.
Treatment - Drugs
Placebo
Intervention: local application of Phenytoin cream 1% once daily in areas susceptible to ulcer (sacrum

Sponsors

Vice-chancellor for Research and Technology, Hamadan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
37 Years to 90 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: patients with 2/5 or more of paralysis due one-way stroke and with pressure ulcer; patients who score 16 or less in Norton scale. Exclusion criteria: patient death or transfer to another health center; patient with necrotic wound due pressure ulcer at the beginning of the study; positive response to allergy test of Q. infectoria gall extract; progression of pressure ulcer to higher grades during the study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Grade of pressure ulcer. Timepoint: At baseline and then daily for two weeks. Method of measurement: Through physical examination.

Secondary

MeasureTime frame
Assessing local reactions such as rash, hives, or redness. Timepoint: 24 hours later. Method of measurement: Through physical examination.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDara Dastan

School of Pharmacy

d.dastan@umsha.ac.ir+98 81 3838 1590

Outcome results

None listed

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