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The effect of electrotherapy modalities on pain and swelling in patients with breast cancer

The effect of ultrasound and Faradic under pressure on upper limb pain, swelling and function in patients with breast cancer after surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201310292391N14
Enrollment
45
Registered
2016-01-03
Start date
2016-01-09
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

breast cancer. Malignant neoplasm of breast

Interventions

Intervention 1: The first group receive conventional therapy (complex decongestive therapy) which includes four stages: gentle massage for lymph drainage, compression therapy with bandages, skin care
Treatment - Other
The first group receive conventional therapy (complex decongestive therapy) which includes four stages: gentle massage for lymph drainage, compression therapy with bandages, skin care and exercise.
The second group, in addition to conventional therapy, receive ultrasound therapy with the intensity of 2 Watt / cm2 and with the frequency of 1 MHz in the arm, forearm and hand.
The third group, in addition to conventional therapy, receive faradic under pressure flow. (frequency 30 Hz, pulse width 300 microsecond, hold time 2 s, rest time 5 s,10 min on the flexors muscle of

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusions criteria: Women with a history of breast cancer for at least the age of 18 ; for at least surgery and chemotherapy or surgery and radiation therapy ; suffering lymph edema Exclusion criteria: Malignancies, including malignant lymph edema, bilateral breast cancer; Cancer or recurrent infection in the arm ; congenital lymph edema ; Patients who for other reasons such as trauma, burns, damage to lymph masses of the region have been affected by lymph edema.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: before treatment and after the tenth session. Method of measurement: numeric analog scale (NAS).;Swelling. Timepoint: before treatment and after the tenth session. Method of measurement: difference in volume between the two sides in various locations and measuring the difference between the volumes of fluid displacement.;Function. Timepoint: before treatment and after the tenth session. Method of measurement: DASH questionnaires (Disability of Arm Shoulder Hand).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZahra Rojhani Shirazi

Shiraz University of Medical Sciences

rojhaniz@sums.ac.ir+98 71 3627 1552

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 13, 2026