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Evaluation the effect of hydrogel on pressure ulcer

Evaluation the effect of hydrogel containing gentamicin on pressure ulcers

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20181105041563N6
Enrollment
105
Registered
2020-12-06
Start date
2020-11-21
Completion date
Unknown
Last updated
2021-01-05

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

Conditions

Pressure ulcer. Stage II decubitus ulcer

Interventions

Intervention 1: First intervention group: in group 1, the wound will be dressed daily at 8:00 AM with hydrogel made by pharmacist researchers of Kermanshah University of Medical Sciences for 30 days,

Sponsors

Kermanshah University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Consent of the physician and the patient to participate in the study No addiction to drugs and alcohol, Insensitivity to hydrogels and gentamicin Absence of any signs of wound infection and skin disease Having aged over 18 years No diabetes, and kidney failure Stage 2 of The National Pressure Ulcer Advisory Panel (NPUAP) scale Lack of bleeding Earn points equal to 14-6 from Braden scale

Exclusion criteria

Exclusion criteria: Earn points more than 18 from Braden scale Administration of nitroglycerin and immunosuppressive drugs Occurrence of pressure ulcer in order to (The National Pressure Ulcer Advisory Panel (NPUAP) scale Need for any surgery Need for debridement Bleeding

Design outcomes

Primary

MeasureTime frame
Healing of pressure ulcer. Timepoint: Day one, three, seven, fourteen, twenty one and thirty of the study. Method of measurement: Push scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSomayeh Mahdavikian

Kermanshah University of Medical Sciences

Somayeh.Mahdavikian@kums.ac.ir+98 83 3816 2560

Outcome results

None listed

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