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Comparative study of the Effects of Emla Cream and Diclofenac Gel on Chemo Port Pain in patients Referring to Oncology wards in Zahedan University of Medical Sciences Affiliated Hospitals

Comparative study of the Effects of Emla Cream and Diclofenac Gel on Chemo Port Pain in patients Referring to Oncology wards in Zahedan University of Medical Sciences Affiliated Hospitals

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017080635520N1
Enrollment
Unknown
Registered
2017-08-30
Start date
2017-03-20
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

cancer. Neoplasms

Interventions

Intervention 1: diclofenac jel .1 geram.1 our once. Intervention 2: emla cream .topical 1 geram.1ouronce. Intervention 3: vitamin(A+D).1 geram.1 our once.
Treatment - Drugs
Placebo
diclofenac jel .1 geram.1 our once
emla cream .topical 1 geram.1ouronce
vitamin(A+D).1 geram.1 our once

Sponsors

Vice chancellor for research Zahedan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to 99 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Inclination to participate in research; Having verbal, subjective, vision ability; At present there is no acute psychiatric disorder; There is no history of favism, congenital idiopathic hemoglobin, liver disease, skin allergy, skin dermatitis; no treatment with sulfonamides, nitrates Phenobarbital, non-diabetes, non-addiction, non-use of housing in the last 24 hours. Exit criteria: The wound of the port's location during the intervention; Infection and secretion at the port site during the intervention; Failure to follow the first action.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Emlacream. Timepoint: During the intervention. Method of measurement: Geram.;Diclofenac gel. Timepoint: During the intervention. Method of measurement: Geram.;Vitamin(A+D). Timepoint: During the intervention. Method of measurement: Geram.

Secondary

MeasureTime frame
Sex. Timepoint: During the intervention. Method of measurement: Patient case.;Duration under chemotherapy. Timepoint: During the intervention. Method of measurement: Day.;Age. Timepoint: During the intervention. Method of measurement: Years.;Severity of pain. Timepoint: During the intervention. Method of measurement: Vas.;Duration of port usage. Timepoint: During the intervention. Method of measurement: Day.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactShima Mohammadinejad

Zahedan Nursing Midwifery Faculty

Sh.mohamadi90@yahoo.com

Outcome results

None listed

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