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The effect of iris on the treatment of phlebitis

The effect of topical ointment of desert iris rhizome extract (Iris songarica Schrenk) on the treatment of phlebitis caused by venous catheters

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210307050612N1
Enrollment
120
Registered
2021-04-20
Start date
2021-05-04
Completion date
Unknown
Last updated
2021-05-26

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

Conditions

Phlebitis. Phlebitis and thrombophlebitis of other sites

Interventions

Intervention 1: Intervention group: The method of intervention will be that in case of signs and symptoms of phlebitis with any degree of peripheral catheter outside and in another place the catheter

Sponsors

Birjand University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
17 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Conscious desire and consent to participate in the study2. Having catheter number 203. Hospitalized in the internal ward of Valiasr Hospital for at least 72 hours4. Insensitivity to glue or medicine5. No blood transfusion6. No systolic blood pressure7. No skin disease in the area of ??phlebitis8. Absence of pregnancy and lactation9. Having at least one of the symptoms of phlebitis (pain, redness, skin irritation) around the area10. Do not use drugs or vegetable oils to treat phlebitis during research11. No history of allergies to plants related to the lily family12. Using the upper limb for catheterization13. Observance of aseptic conditions in catheterization according to the hospital standard

Exclusion criteria

Exclusion criteria: 1. Patients who have been discharged before three days2. Patients with diseases associated with known coagulation status (such as anticardiolipin antibody, antiphospholipid antibody, vitamin deficiency3. Death of the patient4. Unwillingness to cooperate and continue working

Design outcomes

Primary

MeasureTime frame
Phlebitis. Timepoint: Before the intervention, every 12 hours for 72 hours, immediately after the intervention. Method of measurement: Standard VIP instrument (Phlebit degree visual scale).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMassomeh Hossini

Birjand University of Medical Sciences

mashos0953@gmail.com+98 56 3162 6221

Outcome results

None listed

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