Postmastectomy lymphedema Cancer
Conditions
Interventions
Sixty participants were divided into two groups: conventional treatment (CT) group and complete decongestive therapy (CDT) group.
A systematic random sampling procedure was used to include the partic
Sponsors
King Saud University
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: 1. Females aged between 50 and 70 years 2. Unilateral mastectomy for stage I and II breast cancer 3. Completed radiotherapy and chemotherapy sessions 4. Developed lymphedema more than 3cm compared to contralateral extremity
Exclusion criteria
Exclusion criteria: 1. Primary lymphedema 2. Bilateral lymphedema 3. Pulmonary edema 4. Congestive heart failure 5. Contraindications limiting therapy
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Pain measured using the visual analogue score (VAS) at baseline, 4th week and 6th week 2. Health-related Quality of Life, evaluated with the EORTC QLQ C30 and EORTC QLQ-BR23 questionnaires Measurements were taken at baseline, 4 and 6 weeks. | — |
Secondary
| Measure | Time frame |
|---|---|
| Quality of life measured using European Organization of Research and Treatment for Cancer quality of life questionnaire (EORTC QLQ-C30) and the EORTC QLQ-BR23 breast cancer-specific questionnaire. Measured at baseline, 4th week and 6th week. | — |
Countries
India
Outcome results
None listed