CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 10 enrolled
Drug / intervention
questionnairesother
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT05458154
NCT05458154N/ACompleted
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Evaluation and Re-evaluation of Post-mastectomy Pain Syndrome by Breast Cancer EDGE Task Force Outcomes: Clinical Measures of Pain After Pain Management Protocol of Physiotherapy

General Committee of Teaching Hospitals and Institutes, Egypt·interventional·Posted Jul 14, 2022·Updated Jul 14, 2022

In Brief

A clinical study evaluating questionnaires for Post-mastectomy Pain Syndrome. Completed, enrolled 10 participants across 1 site.

Detailed Summary

The purpose of the Breast Cancer EDGE Task Force is to provide physiotherapists with a comprehensive list of outcome measures that can be administered to a selected patient population, to assess post-mastectomy pain syndrome.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsPost-mastectomy Pain Syndrome
CountriesEgypt
Collaborators--

Timeline

N/ACompletedFinished
20222023202420252026
First PostedJul 14, 2022
Enrollment StartMar 3, 2021
Primary CompletionMar 3, 2022
Study CompletionApr 4, 2022
TodayJul 2, 2026
Enrollment to primary: 1 yearPosted 4.0 years ago

Interventions

questionnairesother

Participants were recruited from the Baheya Centre for Early Detection and Treatment of Breast Cancer institution. Patients were eligible if they had a previously post-mastectomy pain syndrome (PMPS), and were presented with pain within the surgical area lasting more than 3 months. They were evaluated by questionnaires and methods of pain assessment then received their physiotherapy program specific for pain relief for six sessions, and so re-evaluation. All women gave informed written consent in Arabic and English forms.