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NCT04676438

Persistant Post-mastectomy Pain in Breast Cancer : Incidence and Risk Factors

Completed Last updated 20 July 2021
What this trial tests

trial in Breast Neoplasms in 722 participants. Completed in 7 March 2021.

Timeline
10 December 2018
Primary endpoint
8 September 2020
7 March 2021

Quick facts

Lead sponsorMoroccan Society of Surgery
StatusCompleted
Study typeOBSERVATIONAL
Enrollment722
Start date10 December 2018
Primary completion8 September 2020
Estimated completion7 March 2021
Sites2 locations across Morocco

Conditions studied

Sponsor

Moroccan Society of Surgery

Who can join

18 and older, female only, with Breast Neoplasms or Pain, Postoperative. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Post Mastectomy Pain Syndrome (PMPS) is a major complication of breast surgery responsible for depression and disability. The project consists of a prospective cohort on patients going for oncological breast surgery at National Institute of Oncology of Rabat. Chronic postoperative pain (CPP) remains a disturbing and obscure clinical problem, which could last for more than 3 months after surgery. The aim of present study was to assess the prevalence of CPP, investigate its impact on life quality and explore its potential risk factors. After informed consent was signed, patients receiving surgery under general anesthesia in Peking Union Medical College Hospital and other medical centers participating in this study during 2018 will be included. Patients' preoperative information will be collected from medical record, including basic demographic data, primary disease and previous chronic diseases. Intraoperative information will be obtained from anesthesia record, including surgical scope, duration, length and location of incisions and blood loss. Acute pain will be evaluated in the ward of the department of surgery, when an app will be installed on patients' mobile phones. Our long-term postoperative follow-up would be performed by sending out survey questionnaires via this app in the 4th, 8th, 16th, 32th, and 48th weeks after surgery. The survey covers questions regarding the intensity, characteristic, location and impact on daily activities of CPP. Information regarding treatment of CPP will also be collected, if any. All the data gained will be summarized in our database and analyzed.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Breast Neoplasms

Currently open trials in the same condition.

Other Moroccan Society of Surgery trials

Trials by the same sponsor.

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Data sources for this page

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