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Mummy effect on the treatment of bedsores

Mummy effect on the healing of bedsores in ICU patients with brain and spinal cord injuries admitted in Shahid Bahonar Education And Treatment Center Of Kerman

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014042917494N1
Enrollment
Unknown
Registered
2015-05-01
Start date
2015-06-10
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

bedsores. diseases of the skin and subcutaeonus tissue

Interventions

Intervention 1: in this interventional study, all ICU patients with brain and spinal cord injuries admitted in Shahid Bahonar Education And Treatment Center Of Kerman who are in the same condition of
Treatment - Drugs
in this interventional study, all ICU patients with brain and spinal cord injuries admitted in Shahid Bahonar Education And Treatment Center Of Kerman who are in the same condition of health care serv
The test group will act like the control group but in addition to physiologic saline, 20 percent Mummy solution will also be used simultaneously and the group will be evaluated similar to the control

Sponsors

Kerman University of Medical Sciences,Vice Chancellor for Research
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 139 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1. Men or women aged 18 years or older; 2. Announcing readiness to go for needed check-ups and remedial measures; 3. Confirm the diagnosis of bedsores of grade 2 or 3 ; 4. Existence of one or more bedsores such that its diameter is less than 15 cm in its widest area; 5. Consent to participate in the study and signing an informed consent form. Exclusion criteria: 1. Any type of pathology (neoplastic, immunological disorders, and etc) on which judgment about the healing process of diabetic foot ulcers is considered as a distracting factor for the researcher; 2. Renal dysfunction to the extent that dialysis treatment is required; 3. Infectious lesions with clinical findings; 4. People with mental or neuronal disorders not capable of cooperating; 5. Refuse signing the informed consent; 6. Worsening of the healing process.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Bedsors. Timepoint: bedsores on days 0, 7, 14, 21 and 28. Method of measurement: Bedsore evaluation is based on the wound surface, secretions and type of tissues. Comparing the collection of these three variables over time will be a template for healing or worsening bedsores.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMasoud Moghadari

Kerman University of Medical Sciences

mmoghadari@kmu.ac.ir+98 34 1223 5011

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Mar 7, 2026