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Effect of Topical Royal on the Improvement of Bedsores

Investigating the Effect of Topical Royal Jelly on the Improvement of Bedsores in Hospitalized Patients in ICU

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240727062554N1
Enrollment
60
Registered
2024-08-17
Start date
2024-08-31
Completion date
Unknown
Last updated
2024-08-26

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

Conditions

Pressure ulcer(Bed sore). Pressure ulcer

Interventions

Intervention 1: Intervention group: To 30 patients with bed sores in the ICU who were enrolled in the study by a wound expert, two days a week for 8 weeks, in addition to the routine treatment of bed

Sponsors

Bagheiat-allah University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: All patients hospitalized in ICU whose bedsores are studied by a wound expert.

Exclusion criteria

Exclusion criteria: Patients who have gangrene. Patients who have osteomyelitis. Patients who have severe sepsis. Patients who have heavy smoking or alcohol consumption. Patients who have liver failure. Patients who have diabetes. Taking drugs that may interfere with the wound healing process (glucocorticoid, immunosuppressive and cytotoxic drugs). Proper follow-up is not done by the patient. The patient does not consent to continue the follow-up. Failure to respond to treatment (wounds that do not respond to treatment after two months are included in this group). The age of the patient is under 18 years.

Design outcomes

Primary

MeasureTime frame
Bed sore healing time. Timepoint: Twice a week for 8 weeks. Method of measurement: The amount of time it takes for the PUSH score to reach zero or one.;The length of the bed sore. Timepoint: Twice a week for 8 weeks. Method of measurement: Using a sterile ruler.;The width of the bed sore. Timepoint: Twice a week for 8 weeks. Method of measurement: Using a sterile ruler.;Bed sore secretions. Timepoint: Twice a week for 8 weeks. Method of measurement: It is classified based on the opinion of the expert and PUSH criteria.;Type of bed sore. Timepoint: Twice a week for 8 weeks. Method of measurement: Based on the expert's observation and opinion, the type of bed sore is classified.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMir Erfan Aribi

Bagheiat-allah University of Medical Sciences

mirerfan.aribi@gmail.com+98 21 8805 0435

Outcome results

None listed

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